{{Rsnum
|rsid=34863047
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=177316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34863047
|variant=0195
}}{{ClinVar
|rsid=34863047
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=227315
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227315G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017214.1
|CLNDBN=HEMOGLOBIN MOSELLA
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=172; 141800.0195
|Disease=HEMOGLOBIN MOSELLA
}}{{PMID Auto
|PMID=8537232
|Title=Three new neutral alpha chain variants: Hb Bois Guillaume [alpha 65(E14(Ala-->Val], Hb Mantes-la-Jolie [alpha 79(EF8)Ala-Thr], and Hb Mosella [alpha 111(G18)Ala-->Thr].
}}