{{Rsnum
|rsid=41491146
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=173161
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141800
|rsnum=41491146
|variant=0052
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000017048.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN HIROSAKI
|CLNHGVS=NC_000016.9:g.223160C>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0052
|Disease=HEMOGLOBIN HIROSAKI
|FwdALT=G
|FwdREF=C
|GENEINFO=HBA2:3040
|GENE_ID=3040
|GENE_NAME=HBA2
|REF=C
|RSPOS=223160
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=127
|rsid=41491146
}}

{{PMID Auto
|PMID=701086
|Title=Further studies on hemoglobin Hirosaki: demonstration of its presence at low concentration.
}}

{{PMID Auto
|PMID=1182166
|Title=Hemoglobin Hirosaki (alpha 43 [CE 1] Phe replaced by Leu), a new unstable variant.
}}

{{PMID Auto
|PMID=1954347
|Title=Further cases of Hb Hirosaki in two Japanese families.
}}

{{on chip | 23andMe v4}}