{{Rsnum
|rsid = 28928883
|Gene=HBA2
|Orientation=plus
|geno1 = (A;A)
|geno2 = (A;C)
|geno3 = (C;C)
|ReferenceAllele=A
|MissenseAllele=G
|Chromosome=16
|position=176970
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|desc=HEMOGLOBIN OITA
|id=141800
|rsnum=28928883
|variant=0201
}}
{{ neighbor
| rsid = 28928886
| distance = 14
}}
{{ neighbor
| rsid = 28928878
| distance = 42
}}
{{omim
|id=141800
|rsnum=28928883
|variant=0034
}}{{ClinVar
|rsid=28928883
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=226969
|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.226969A>C; NC_000016.9:g.226969A>G
|CLNORIGIN=1
|CLNSRCID=
62; 141800.0201; 59; 141800.0034
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017220.1; RCV000017021.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN OITA; HEMOGLOBIN FORT DE FRANCE
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN OITA; HEMOGLOBIN FORT DE FRANCE
}}{{PMID Auto
|PMID=18205
|Title=Hemoglobin Fort de France (alpha2(45)(CD3) His replaced by Arg beta2). A new variant with increased oxygen affinity.
}}

{{PMID Auto
|PMID=2752146
|Title=Locus assignment of two alpha-globin structural mutants from the Caribbean basin: alpha Fort de France (alpha 45 Arg) and alpha Spanish Town (alpha 27 Val).
}}