{{Rsnum
|rsid=33951465
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226947
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33951465
|variant=0369
}}{{ClinVar
|rsid=33951465
|Reversed=1
|FwdREF=T
|FwdALT=A,G
|REF=A
|ALT=C,T
|RSPOS=5248177
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000040402110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5248177A>T
|CLNSRC=GTR; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000500319; NBK1426; 141900.0369
|CLNSIG=5
|CLNCUI=C0039730
|CLNDBN=Beta-plus-thalassemia; alpha Thalassemia; beta Thalassemia
|Disease=Beta-plus-thalassemia; alpha Thalassemia; beta Thalassemia
|CLNACC=RCV000016717.24; RCV000020339.1; RCV000030002.1
|Tags=RV;PM;PMC;S3D;SLO;VLD;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001; NBK1426:C0005283:613985:848:65959000
}}{{PMID Auto
|PMID=2458145
|Title=Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.
}}

{{PMID Auto
|PMID=2634667
|Title=Characterization of beta-thalassemia mutations among the Japanese.
}}

{{PMID Auto
|PMID=6572978
|Title="Silent" nucleotide substitution in a beta+-thalassemia globin gene activates splice site in coding sequence RNA.
|OA=1
}}

{{PMID Auto
|PMID=6188062
|Title=Specific transcription and RNA splicing defects in five cloned beta-thalassaemia genes.
}}

{{PMID Auto
|PMID=6583702
|Title=beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.
|OA=1
}}

{{PMID Auto
|PMID=20737602
|Title=Molecular characterization of sickle cell anemia in the Northern Brazilian state of Para.
}}