{{Rsnum
|rsid=33949106
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBA2
|position=177003
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33949106
|variant=0147
}}
{{omim
|id=141800
|rsnum=33949106
|variant=0164
}}{{ClinVar
|rsid=33949106
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=227002
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.227002A>C; NC_000016.9:g.227002A>G
|CLNORIGIN=1
|CLNSRCID=
79; 141800.0147; 82; 141800.0164
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017166.1; RCV000017185.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN THAILAND; HEMOGLOBIN PORT HURON
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN THAILAND; HEMOGLOBIN PORT HURON
}}{{PMID Auto
|PMID=604316
|Title=Hemoglobin Thailand [alpha 56 (E 5) Lys leads to Thr]: a new abnormal human hemoglobin.
}}

{{PMID Auto
|PMID=1802882
|Title=Hb Port Huron [alpha 56 (E5)Lys----ARG]: a new alpha chain variant.
}}