{{Rsnum
|rsid=35723200
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA1
|position=177403
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=35723200
|variant=0182
}}

{{ClinVar
|rsid=35723200
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=227402
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000a01000502110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227402T>C
|CLNORIGIN=1
|CLNSIG=1
|Tags=PM;PMC;S3D;SLO;NSM;REF;HD;GNO;OTHERKG;LSD;OM
}}

{{PMID Auto
|PMID=1390944
|Title=Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity.
}}

{{PMID Auto
|PMID=1428951
|Title=Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}