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, NR_001589.1
Associated with diseases HBFQTL-1
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 161
Unique public DNA variants reported 10
Individuals with public variants 35
Hidden variants 17
Date created November 30, -0001
Date last updated September 28, 2016
Version HBG1:160928

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:4831
Entrez Gene 3047
PubMed articles HBG1
OMIM - Gene 142200
OMIM - Diseases HBFQTL-1 (hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00011958 11 hemoglobin, gamma A NM_000559.2 NP_000550.2 161
00031612 11 Manually created transcript (removed from reference sequence) NR_001589.1 - -