{{Rsnum
|rsid=63749948
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBA1
|position=177314
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=63749948
|variant=0117
}}{{ClinVar
|rsid=63749948
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=227313
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000a01000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.227313C>A; NC_000016.9:g.227313C>T
|CLNORIGIN=1
|CLNSIG=1
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=7470621
|Title=Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression.
}}