{{Rsnum
|rsid=33914668
|Gene=HBB
|Chromosome=11
|position=5225728
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33914668
|variant=0353
}}
{{omim
|id=141900
|rsnum=33914668
|variant=0354
}}

{{ClinVar
|rsid=33914668
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=5246958
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000416110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5246958T>C; NC_000011.9:g.5246958T>G
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; NBK1426; 940
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000020336.1; RCV000020335.1
|Tags=RV;PM;PMC;SLO;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591; .
|CLNDBN=alpha Thalassemia
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001
|CLNSRC=GTR; GeneReviews; HBVAR
|COMMON=0
|Disease=alpha Thalassemia
}}

{{PMID Auto
|PMID=2424301
|Title=The beta zero-thalassemia in an American black family is due to a single nucleotide substitution in the acceptor splice junction of the second intervening sequence.
}}

{{PMID Auto
|PMID=2123063
|Title=Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia allele.
}}

{{PMID Auto
|PMID=2987809
|Title=Beta-thalassemia resulting from a single nucleotide substitution in an acceptor splice site.
|OA=1
}}

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

{{on chip | HumanOmni1Quad}}