View HBB gene homepage

General information
Gene symbol HBB
Gene name hemoglobin subunit beta
Chromosome 11
Chromosomal band p15.5
Imprinted Unknown
Genomic reference NG_000007.3
Transcript reference NM_000518.4
Associated with diseases HPFH, SCD, β-Thal
Citation reference(s) -
Curators (1) Carsten W Lederer
Total number of public variants reported 19
Unique public DNA variants reported 17
Individuals with public variants 0
Hidden variants 0
Date created June 07, 2016
Date last updated July 01, 2016
Version HBB:160701

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL http://www.ithanet.eu
HGNC 4827
Entrez Gene 3043
PubMed articles HBB
OMIM - Gene 141900
OMIM - Diseases HPFH (Hereditary Persistence of Fetal Hemoglobin)
SCD (Sickle Cell Disease)
β-Thal (β-thalassaemia)
HGMD HBB
GeneCards HBB
GeneTests HBB


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000078 11 hemoglobin, beta NM_000518.4 NP_000509.1 19


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