{{Rsnum
|rsid=33984024
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=177026
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33984024
|variant=0043
}}
{{omim
|id=141800
|rsnum=33984024
|variant=0116
}}
{{omim
|id=141800
|rsnum=33984024
|variant=0121
}}{{ClinVar
|rsid=33984024
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=227025
|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.227025G>A; NC_000016.9:g.227025G>C; NC_000016.9:g.227025G>T
|CLNORIGIN=1
|CLNSRCID=
141800.0043; 97; 141800.0121; 96; 141800.0116
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017034.1; RCV000017035.1; RCV000017144.1; RCV000017139.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN G (WAIMANALO); HEMOGLOBIN AIDA; HEMOGLOBIN Q (INDIA); HEMOGLOBIN PERSPOLIS
|CLNSRC=OMIM Allelic Variant; HBVAR
|Disease=HEMOGLOBIN G (WAIMANALO); HEMOGLOBIN AIDA; HEMOGLOBIN Q (INDIA); HEMOGLOBIN PERSPOLIS
}}{{PMID Auto
|PMID=1259994
|Title=Two new haemoglobins: haemoglobin Perspolis (alpha 64 (E13) Asp leads to Tyr) and haemoglobin J-Kurosh (alpha 19 (AB) Ala leads to Asp).
}}

{{PMID Auto
|PMID=949043
|Title=Hemoglobin QIndia, alpha 64 (E13) Asp replaced by His, and beta-thalassemia in a Canadian family.
}}

{{PMID Auto
|PMID=4646552
|Title=Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families.
|OA=1
}}

{{PMID Auto
|PMID=6585831
|Title=beta-Thalassemia in Chinese: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects.
|OA=1
}}