The HBG2 gene homepage

General information
Gene symbol HBG2
Gene name hemoglobin, gamma G
Chromosome 11
Chromosomal band p15.5
Imprinted Unknown
Genomic reference NG_000007.3
Transcript reference NM_000184.2
Associated with diseases HBFQTL-1, Cyanosis, transient neonatal
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 169
Unique public DNA variants reported 9
Individuals with public variants 35
Hidden variants 1
Date created November 30, -0001
Date last updated September 28, 2016
Version HBG2:160928

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:4832
Entrez Gene 3048
PubMed articles HBG2
OMIM - Gene 142250
OMIM - Diseases HBFQTL-1 (hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1))
Cyanosis, transient neonatal


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00011959 11 hemoglobin, gamma G NM_000184.2 NP_000175.1 169