{{Rsnum
|rsid=33977363
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=177059
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33977363
|variant=0095
}}
{{omim
|id=141800
|rsnum=33977363
|variant=0122
}}
{{omim
|id=141800
|rsnum=33977363
|variant=0157
}}{{ClinVar
|rsid=33977363
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=227058
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000016.9:g.227058G>A; NC_000016.9:g.227058G>C; NC_000016.9:g.227058G>T
|CLNORIGIN=1
|CLNSRCID=
114; 141800.0095; 111; 141800.0122; 113; 141800.0157
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017107.1; RCV000017145.1; RCV000017179.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN MATSUE-OKI; HEMOGLOBIN Q (IRAN); HEMOGLOBIN WINNIPEG
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN MATSUE-OKI; HEMOGLOBIN Q (IRAN); HEMOGLOBIN WINNIPEG
}}{{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=3754247
|Title=Some notes about Hb Q-India and Hb Q-Iran.
}}

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

{{PMID Auto
|PMID=4728965
|Title=Hemoglobin Winnipeg: alpha2 75 Asp leads to Tyr beta2.
}}

{{PMID Auto
|PMID=6841125
|Title=Hb Winnipeg or alpha 2 75(EF4)Asp leads to Tyr beta 2 in a large Caucasian family living in Georgia, USA.
}}

{{PMID Auto
|PMID=640845
|Title=Hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black American.
}}

{{PMID Auto
|PMID=893135
|Title=Hemoglobin Matsue-Oki: alpha 75 (EF 4) aspartic acid leads to asparagine.
}}

{{PMID Auto
|PMID=6814490
|Title=Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant.
}}