{{Rsnum
|rsid=33980857
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5227101
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33980857
|variant=0377
}}
{{omim
|id=141900
|rsnum=33980857
|variant=0378
}}{{ClinVar
|rsid=33980857
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248331
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=3
|CLNHGVS=NC_000011.9:g.5248331A>T
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; 765; 141900.0377
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016725.24; RCV000029962.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=Beta-plus-thalassemia; beta Thalassemia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|Disease=Beta-plus-thalassemia; beta Thalassemia
}}{{PMID Auto
|PMID=1917531
|Title=Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
}}

{{PMID Auto
|PMID=3382401
|Title=Beta-thalassemia due to a T----A mutation within the ATA box.
}}

{{PMID Auto
|PMID=2741940
|Title=A new TATA box mutation detected at prenatal diagnosis for beta-thalassemia.
|OA=1
}}