Human (GRCh37.p13)
Description

hemoglobin, gamma G [Source:HGNC Symbol;Acc:4832]

Gene Synonyms

TNCY

Location

Chromosome 11: 5,274,420-5,667,019 reverse strand.

GRCh37:CM000673.1

About this gene

This gene has 4 transcripts (splice variants), 9 paralogues and is associated with 4 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000380259.2HBG2-0011772147aa
 
Protein coding
CCDS7755A1EGU3 D9YZU9 P69892
Q14402 Q14474 Q14476
Q9UJ01 Q9UNL6
-Ensembl CanonicalGENCODE Basic
ENST00000380252.1HBG2-004694137aa
 
Protein coding
A1EGU3 E9PBW4 Q14402
Q9UJ01
-GENCODE Basic
ENST00000336906.4HBG2-201602147aa
 
Protein coding
CCDS7755A1EGU3 D9YZU9 P69892
Q14402 Q14474 Q14476
Q9UJ01 Q9UNL6
NM_000184.2GENCODE Basic
ENST00000444587.1HBG2-00330730aa
 
Nonsense mediated decay
F8WB96 --
Name

HBG2 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P69892

CCDS

This gene is a member of the Human CCDS set: CCDS7755.1

Ensembl version

ENSG00000196565.8

Other assemblies

This gene maps to 5,253,190-5,645,789 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000066673 (version 6)

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