{{Rsnum
|rsid=34988734
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA1
|position=177101
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34988734
|variant=0213
}}

{{ClinVar
|rsid=34988734
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=227100
|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.227100C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017232.1
|CLNDBN=HEMOGLOBIN VILLEURBANNE
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=140; 141800.0213
|Disease=HEMOGLOBIN VILLEURBANNE
}}

{{PMID Auto
|PMID=9269086
|Title=Combined mass spectrometric methods for the characterization of human hemoglobin variants localized within alpha T9 peptide: identification of Hb Villeurbanne alpha 89 (FG1) His-->Tyr.
}}

{{on chip | 23andMe v3}}