The HBG1 gene homepage

General information
Gene symbol HBG1
Gene name hemoglobin, gamma A
Chromosome 11
Chromosomal band p15.5
Imprinted Unknown
Genomic reference NG_000007.3
Transcript reference NM_000559.2
Exon/intron information NM_000559.2 exon/intron table
Associated with diseases HBFQTL1, thal
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 61
Unique public DNA variants reported 60
Individuals with public variants 55
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created November 06, 2008
Date last updated April 16, 2023
Version HBG1:230416

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_000559.2.
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 https://www.LOVD.nl/HBG1
External URL HbVar - human hemoglobin variants and thalassemias
The Globin Gene Server
HGNC 4831
Entrez Gene 3047
PubMed articles HBG1
OMIM - Gene 142200
OMIM - Diseases HBFQTL1 (hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1))
HGMD HBG1
GeneCards HBG1
GeneTests HBG1
Orphanet HBG1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00009176 11 hemoglobin, gamma A NM_000559.2 NP_000550.2 61


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