{{Rsnum
|rsid=33961916
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=176735
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33961916
|variant=0029
}}
{{omim
|id=141800
|rsnum=33961916
|variant=0158
}}{{ClinVar
|rsid=33961916
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=226734
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 3
|CLNHGVS=NC_000016.9:g.226734G>A; NC_000016.9:g.226734G>T
|CLNORIGIN=1
|CLNSRCID=
6; 141800.0029; 8; 141800.0158
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017016.1; RCV000017180.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN DUNN; HEMOGLOBIN WOODVILLE
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN DUNN; HEMOGLOBIN WOODVILLE
}}{{PMID Auto
|PMID=478975
|Title=Hemoglobin Dunn: alpha 6 (A4) aspartic acid replaced by asparagine.
}}

{{PMID Auto
|PMID=3354560
|Title=Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan man.
}}

{{PMID Auto
|PMID=6668192
|Title=Two rare alpha chain variants, Hb Dunn or alpha 26(A4)Asp replaced by Asn beta 2 and Hb G-Pest or alpha 274(EF3)Asp replaced by Asn beta 2, observed in an Indian and a black newborn.
}}

{{PMID Auto
|PMID=7435503
|Title=Oxygen affinity and stability of hemoglobin Dunn alpha 6(A4)Asp replaced by Asn): use of isoelectric focusing in recognition of a new abnormal hemoglobin.
}}

{{PMID Auto
|PMID=3754246
|Title=Hemoglobin Woodville: alpha (2)6(A4) aspartic acid----tyrosine.
}}