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
Exon/intron information NM_000184.2 exon/intron table
Associated with diseases HBFQTL-1, thal, Cyanosis, transient neonatal
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 80
Unique public DNA variants reported 79
Individuals with public variants 75
Hidden variants 1
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 September 17, 2021
Version HBG2:210917

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_000184.2.
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
External URL HbVar - human hemoglobin variants and thalassemias
The Globin Gene Server
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
GeneCards HBG2
GeneTests HBG2
Orphanet HBG2

Active transcripts




NCBI ID     

NCBI Protein ID     

00009177 11 hemoglobin, gamma G NM_000184.2 NP_000175.1 80

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