{{Rsnum
|rsid=33941849
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5227020
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33941849
|variant=0344
}}
{{omim
|id=141900
|rsnum=33941849
|variant=0345
}}{{ClinVar
|rsid=33941849
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248250
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5248250A>C; NC_000011.9:g.5248250A>G
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; 141900.0344; 141900.0345
|CLNSIG=5
|CLNCUI=
|CLNDBN=beta0^ Thalassemia; Beta-thalassemia, lermontov type; beta Thalassemia
|Disease=beta0^ Thalassemia; Beta-thalassemia; beta Thalassemia
|CLNACC=
RCV000016691.24; RCV000016692.24; RCV000016693.24; RCV000029976.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271980:86715000; NBK1426:C0005283:613985:848:65959000
}}{{PMID Auto
|PMID=211197
|Title=Herpes simplex virus necleic acid synthesis following infection of non-permissive XC cells.
}}

{{PMID Auto
|PMID=9101288
|Title=beta-thalassemia mutations in Japanese and Koreans.
}}

{{PMID Auto
|PMID=10815781
|Title=Beta-thalassaemia in Cubans: novel allele increases the genetic diversity at the HBB locus in the Caribbean.
}}

{{PMID Auto
|PMID=12709369
|Title=Rapid detection of beta-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis.
}}

{{PMID Auto
|PMID=18294253
|Title=Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity.
}}

{{PMID Auto
|PMID=19254853
|Title=Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
}}{{PMID Auto
|PMID=2272840
|Title=An initiation codon mutation as a cause of a beta-thalassemia.
}}

{{PMID Auto
|PMID=1517111
|Title=A beta-thalassemia mutation found in Korea.
}}

{{PMID Auto
|PMID=2306523
|Title=A new single nucleotide change at the initiation codon (ATG----AGG) identified in amplified genomic DNA of a Chinese beta-thalassemic patient.
}}

{{PMID Auto
|PMID=16114187
|Title=A mutation of the beta-globin gene initiation codon, ATG-->AAG, found in a French Caucasian man.
}}