{{Rsnum
|rsid=33944813
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBA1
|position=177102
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33944813
|variant=0172
}}
{{omim
|id=141800
|rsnum=33944813
|variant=0214
}}
{{omim
|id=141800
|rsnum=33944813
|variant=0215
}}{{ClinVar
|rsid=33944813
|Reversed=0
|FwdREF=A
|FwdALT=C,G,T
|REF=A
|ALT=C,G,T
|RSPOS=227101
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000016.9:g.227101A>C; NC_000016.9:g.227101A>G; NC_000016.9:g.227101A>T
|CLNORIGIN=1
|CLNSRCID=
141; 141800.0214; 1109; 141800.0215; 139; 141800.0172
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017233.1; RCV000017234.1; RCV000017192.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN TOKYO; HEMOGLOBIN TAMANO; HEMOGLOBIN LUTON
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN TOKYO; HEMOGLOBIN TAMANO; HEMOGLOBIN LUTON
}}{{PMID Auto
|PMID=1486044
|Title=Polycythaemia and microcytosis arising from the combination of a new high oxygen affinity haemoglobin (Hb luton, alpha 89 His-->Leu) and alpha thalassaemia trait.
}}