{{Rsnum
|rsid=63749934
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA2
|position=173196
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=63749934
|variant=0046
}}

{{ClinVar
|rsid=63749934
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=223195
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223195T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016956.1
|CLNDBN=HEMOGLOBIN GERLAND
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141850.0046
|Disease=HEMOGLOBIN GERLAND
}}

{{PMID Auto
|PMID=11791875
|Title=Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}