{{Rsnum
|rsid = 28928875
|Gene=HBA2
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=16
|position=177056
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|desc=HEMOGLOBIN G (PEST)
|id=141800
|rsnum=28928875
|variant=0041
}}
{{omim
|desc=HEMOGLOBIN G (TAICHUNG)
|id=141800
|rsnum=28928875
|variant=0042
}}
{{omim
| id = 141800
| variant = 0095
| desc    = HEMOGLOBIN MATSUE-OKI
| rsnum   = 28928875
}}
{{omim
| id = 141800
| variant = 0122
| desc    = HEMOGLOBIN Q (IRAN)
| rsnum   = 28928875
}}
{{ neighbor
| rsid = 28928882
| distance = 4
}}
{{ neighbor
| rsid = 28928876
| distance = 39
}}{{ClinVar
|rsid=28928875
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=227055
|CHROM=16
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.227055G>A; NC_000016.9:g.227055G>C
|CLNORIGIN=1
|CLNSRCID=
141800.0041; 141800.0042
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017027.1; RCV000017028.1; RCV000017029.1; RCV000017030.1; RCV000017031.1; RCV000017032.1; RCV000017033.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN G (PEST); HEMOGLOBIN G (TAICHUNG); HEMOGLOBIN Q; HEMOGLOBIN Q (THAILAND); HEMOGLOBIN MAHIDOL; HEMOGLOBIN ASABARA; HEMOGLOBIN KURASHIKI
|CLNSRC=OMIM Allelic Variant
|Disease=HEMOGLOBIN G (PEST); HEMOGLOBIN G (TAICHUNG); HEMOGLOBIN Q; HEMOGLOBIN Q (THAILAND); HEMOGLOBIN MAHIDOL; HEMOGLOBIN ASABARA; HEMOGLOBIN KURASHIKI
}}{{PMID Auto
|PMID=508945
|Title=The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
}}

{{PMID Auto
|PMID=640847
|Title=Hemoglobin G Taichung (alpha 74 aspartic acid replaced by histidine) heterozygotes found in two Japanese families.
}}

{{PMID Auto
|PMID=1428945
|Title=A case of -(4.2)alpha T/-(4.2) alpha Q in combination with a beta zero-thalassemia homozygosity found in a family of the Zhuang nationality in china.
}}

{{PMID Auto
|PMID=2882671
|Title=HB Q-Thailand-HB H disease in a Chinese living in Geneva, Switzerland: characterization of the variant and identification of the two alpha-thalassemic chromosomes.
}}

{{PMID Auto
|PMID=5410724
|Title=Hemoglobin G Taichung: alpha-74 Asp leads to His.
}}

{{PMID Auto
|PMID=5460202
|Title=Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine.
}}

{{PMID Auto
|PMID=5475469
|Title=Hemoglobin Mahidol: a new hemoglobin alpha-chain mutant.
}}

{{PMID Auto
|PMID=7448125
|Title=The genetic basis of Hb Q-H disease.
}}

{{PMID Auto
|PMID=7803274
|Title=The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.
}}

{{PMID Auto
|PMID=4550395
|Title=Multiple alpha chain loci for human haemoglobins: Hb J-Buda and Hb G-Pest.
}}