{{Rsnum
|rsid=33926206
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBA2
|position=177086
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33926206
|variant=0030
}}{{ClinVar
|ALT=C,G
|CHROM=16
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227085A>C
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=C,G
|FwdREF=A
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=A
|RSPOS=227085
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=33926206
|CLNACC=RCV000017017.1
|CLNDBN=HEMOGLOBIN ETOBICOKE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0030
|Disease=HEMOGLOBIN ETOBICOKE
}}{{PMID Auto
|PMID=5774804
|Title=Hemoglobin Etobicoke: alpha-84(F5) serine replaced by arginine.
}}

{{PMID Auto
|PMID=6874377
|Title=Hb Etobicoke, alpha 85(F5) Ser leads to Arg found in a newborn of French-Indian-English descent.
}}