{{Rsnum
|rsid=35974739
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA1
|position=177376
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=35974739
|variant=0167
}}{{ClinVar
|rsid=35974739
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=227375
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000a01000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227375T>C
|CLNORIGIN=1
|CLNSIG=1
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
}}

{{PMID Auto
|PMID=7717382
|Title=Hb Questembert is due to a base substitution (T-->C) in codon 131 of the alpha 2-globin gene and has an alpha-thalassemia biosynthetic ratio.
}}

{{PMID Auto
|PMID=8493987
|Title=Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly).
}}

{{on chip | 23andMe v4}}