{{Rsnum
|rsid=34220980
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=176717
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141850
|rsnum=34220980
|variant=0022
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.226716A>G
|CLNORIGIN=1
|CLNSIG=1
|FwdALT=G
|FwdREF=A
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=A
|RSPOS=226716
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000a01000002110100
|WGT=1
|dbSNPBuildID=126
|rsid=34220980
}}{{PMID Auto
|PMID=3680504
|Title=An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype.
|OA=1
}}