{{Rsnum
|rsid = 28928889
|Gene=HBA2
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=16
|position=173503
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|desc=HEMOGLOBIN ANAMOSA
|id=141850
|rsnum=28928889
|variant=0029
}}
{{ neighbor
| rsid = 1061009
| distance = 204
}}

{{ClinVar
|rsid=28928889
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=223502
|CHROM=16
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000016.9:g.223502C>T
|CLNORIGIN=1
|CLNSRCID=
141850.0029
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016940.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN ANAMOSA
|CLNSRC=OMIM Allelic Variant
|Disease=HEMOGLOBIN ANAMOSA
}}

{{PMID Auto
|PMID=7470621
|Title=Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}