{{Rsnum
|rsid = 28928885
|Gene=HBA2
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=16
|position=176746
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|desc=HEMOGLOBIN DELFZICHT
|id=141800
|rsnum=28928885
|variant=0208
}}
{{ neighbor
| rsid = 28928888
| distance = 28
}}
{{ neighbor
| rsid = 28928880
| distance = 44
}}

{{omim
|id=141850
|rsnum=28928885
|variant=0048
}}

{{ClinVar
|rsid=28928885
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=226745
|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
|CLNHGVS=NC_000016.9:g.226745C>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017227.1
|CLNDBN=HEMOGLOBIN DELFZICHT
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=1122; 141800.0208
|Disease=HEMOGLOBIN DELFZICHT
}}

{{PMID Auto
|PMID=12144062
|Title=Hb delfzicht [alpha9(A7)Asn-->Lys (alpha1)]: a new, clinically silent hemoglobin variant observed in a Dutch patient.
}}

{{on chip | 23andMe v3}}