{{Rsnum
|rsid=33935673
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5225689
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33935673
|variant=0213
}}
{{omim
|id=141900
|rsnum=33935673
|variant=0250
}}{{ClinVar
|rsid=33935673
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=5246919
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246919T>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=1
|CLNCUI=
|CLNDBN=beta Thalassemia
|Disease=beta Thalassemia
|CLNACC=
RCV000029992.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
}}{{PMID Auto
|PMID=700140
|Title=The hemoglobin P-Galveston-Hb-C conduction in members of a black family from South Carolina.
}}

{{PMID Auto
|PMID=1164567
|Title=A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.
}}

{{PMID Auto
|PMID=10870891
|Title=Identification of the nucleotide change (CAC-->CGC) responsible for Hb P-Galveston [BETA117(G19)His-->Arg].
}}

{{PMID Auto
|PMID=12386379
|Title=Diagnosis of Hemoglobinopathies by High-Performance Liquid Chromatography.
}}

{{PMID Auto
|PMID=14109943
|Title=HAEMOGLOBINS N AND P IN ITALIAN FAMILIES.
}}

{{PMID Auto
|PMID=20395516
|Title=Comprehensive and efficient HBB mutation analysis for detection of beta-hemoglobinopathies in a pan-ethnic population.
}}{{PMID Auto
|PMID=5775133
|Title=Hemoglobin P (alpha 2 beta 2 117 Arg): structure and properties.
}}

{{PMID Auto
|PMID=6687721
|Title=Hemoglobin saitama or beta 117 (G19) His leads to Pro, a new variant causing hemolytic disease.
}}