{{Rsnum
|rsid=33944368
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBA2
|position=176976
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33944368
|variant=0023
}}
{{omim
|id=141800
|rsnum=33944368
|variant=0084
}}{{ClinVar
|rsid=33944368
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=226975
|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.226975A>C; NC_000016.9:g.226975A>G
|CLNORIGIN=1
|CLNSRCID=
67; 141800.0023; 64; 141800.0084
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017010.1; RCV000017083.1; RCV000017084.1; RCV000017085.1; RCV000017086.1; RCV000017087.1; RCV000017088.1; RCV000017089.1; RCV000017090.1; RCV000017091.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN CORDELE; HEMOGLOBIN KOKURA; HEMOGLOBIN BEILINSON; HEMOGLOBIN MICHIGAN-I; HEMOGLOBIN MICHIGAN-II; HEMOGLOBIN L (GASLINI); HEMOGLOBIN TAGAWA II; HEMOGLOBIN UMI; HEMOGLOBIN MUGINO; HEMOGLOBIN YUKUHASHI-2
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN CORDELE; HEMOGLOBIN KOKURA; HEMOGLOBIN BEILINSON; HEMOGLOBIN MICHIGAN-I; HEMOGLOBIN MICHIGAN-II; HEMOGLOBIN L (GASLINI); HEMOGLOBIN TAGAWA II; HEMOGLOBIN UMI; HEMOGLOBIN MUGINO; HEMOGLOBIN YUKUHASHI-2
}}{{PMID Auto
|PMID=7068437
|Title=HB Kokura [alpha 47 (CE 5) Asp leads to Gly]: a slightly unstable variant.
}}

{{PMID Auto
|PMID=6547117
|Title=Hb Cordele alpha(2)47 (CE5)Asp----Ala beta 2. A mildly unstable variant observed in black twins.
}}