Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HBG2 ENSPTRG00000043688

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Description

hemoglobin, gamma G [Source:NCBI gene (formerly Entrezgene);Acc:450979]

Location

Chromosome 11: 5,020,432-5,298,800 reverse strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 2 transcripts (splice variants), 542 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000066372.2	HBG2-201	444	147aa	ENSPTRP00000057950.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8P6N7 P61921	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSPTRT00000062292.3	HBG2-202	414	137aa	ENSPTRP00000054848.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XGJ3 H2RB13	-

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Summary

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