{{Rsnum
|rsid=33991059
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5226779
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33991059
|variant=0109
}}{{ClinVar
|rsid=33991059
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=5248009
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248009C>G
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016382.1
|CLNDBN=HEMOGLOBIN HIROSE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0109
|Disease=HEMOGLOBIN HIROSE
}}{{PMID Auto
|PMID=5056652
|Title=Oxygen equilibrium characteristics of abnormal hemoglobins. Hirose (alpha-2-beta-2-37Ser), L Ferrara (alpha-2-47-Gly-beta-2), Broussais (alpha-2-90-Asn-beta-2), and Dhofar (alpha-2-beta-2-58Arg).
|OA=1
}}

{{PMID Auto
|PMID=5126162
|Title=Hemoglobin Hirose: 2 237(C3) tryptophan yielding serine.
}}

{{PMID Auto
|PMID=6671905
|Title=Two further examples of Hb Hirose, beta 37 (C3) Trp----Ser.
}}

{{PMID Auto
|PMID=16114184
|Title=Beta-thalassemia due to a novel nonsense mutation at codon 37 (TGG-->TAG) found in an Afghanistani family.
}}