{{Rsnum
|rsid=33986703
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226970
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33986703
|variant=0192
}}
{{omim
|id=141900
|rsnum=33986703
|variant=0311
}}
{{omim
|id=141900
|rsnum=33986703
|variant=0411
}}{{ClinVar
|rsid=33986703
|Reversed=1
|FwdREF=A
|FwdALT=C,G,T
|REF=T
|ALT=A,C,G
|RSPOS=5248200
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000402110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248200T>A
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; NBK1426; 800; 141900.0311
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016655.24; RCV000020337.1
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM;NOV
|CLNDBN=beta0^ Thalassemia; alpha Thalassemia
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271980:86715000; NBK1426:NBK1435:C0002312:604131:846:68913001
|CLNSRC=GTR; GeneReviews; HBVAR; OMIM Allelic Variant
|Disease=beta0^ Thalassemia; alpha Thalassemia
}}{{PMID|88735|OA=1
}} beta 0 thalassemia, a nonsense mutation in man.

{{PMID|10612821}} Human gene mutation database-a biomedical information and research resource.

{{PMID Auto
|PMID=9101287
|Title=Hb Nagasaki [beta 17 (A14)Lys-->Glu]: a second case found in a Japanese family.
}}

{{PMID Auto
|PMID=2737920
|Title=Some abnormal hemoglobin identifications in the U.S.S.R. by micropreparative thin layer peptide mapping.
}}

{{on chip | 23andMe v4}}