{{Rsnum
|rsid = 28928878
|Gene=HBA2
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=16
|position=177012
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|desc=HEMOGLOBIN ADANA
|id=141800
|rsnum=28928878
|variant=0174
}}
{{ neighbor
| rsid = 28928883
| distance = 42
}}
{{ neighbor
| rsid = 28928887
| distance = 4
}}
{{omim
|id=141800
|rsnum=28928878
|variant=0151
}}{{ClinVar
|rsid=28928878
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=227011
|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.227011G>A; NC_000016.9:g.227011G>T
|CLNORIGIN=1
|CLNSRCID=
87; 141800.0174; 86; 141800.0151
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017194.1; RCV000022600.1; RCV000017170.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN ADANA; Hemoglobin H disease, nondeletional; HEMOGLOBIN TOTTORI
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN ADANA; Hemoglobin H disease; HEMOGLOBIN TOTTORI
}}{{PMID Auto
|PMID=7275660
|Title=Hemoglobin Tottori (alpha 59[E8] glycine replaced by valine).
}}

{{PMID Auto
|PMID=868864
|Title=alpha-Thalassemia and beta-thalassemia in a Turkish family.
}}

{{PMID Auto
|PMID=8237999
|Title=Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
}}

{{PMID Auto
|PMID=9029003
|Title=Molecular defects in Hb H hydrops fetalis.
}}