{{Rsnum
|rsid=36015961
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5225698
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=36015961
|variant=0424
}}

{{ClinVar
|rsid=36015961
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=5246928
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000502110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246928A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=141900.0424
|CLNSIG=255
|CLNCUI=C0472767
|CLNDBN=Beta thalassemia intermedia; HEMOGLOBIN BRESCIA; HEMOGLOBIN DURHAM-N.C.
|Disease=Beta thalassemia intermedia; HEMOGLOBIN BRESCIA; HEMOGLOBIN DURHAM-N.C.
|CLNACC=RCV000016775.24; RCV000016776.1; RCV000016777.1
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0472767:191189009
}}

{{PMID Auto
|PMID=8037185
|Title=Beta-thalassemia alleles and unstable hemoglobin types among Russian pediatric patients.
}}

{{PMID Auto
|PMID=8111050
|Title=A novel beta-globin mutation, beta Durham-NC [beta 114 Leu-->Pro], produces a dominant thalassemia-like phenotype.
}}

{{PMID Auto
|PMID=11300352
|Title=A Korean family with a dominantly inherited beta-thalassemia due to Hb Durham-N.C./Brescia.
}}

{{on chip | 23andMe v3}}
{{on chip | HumanOmni1Quad}}