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

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Gene: CHGB ENSOCUG00000028039

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Description

chromogranin B [Source:HGNC Symbol;Acc:HGNC:1930]

Location

Chromosome 4: 12,357,146-12,366,948 forward strand.

OryCun2.0:CM000793.1

About this gene

This gene has 1 transcript (splice variant), 122 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000031929.2	CHGB-201	1929	642aa	ENSOCUP00000024926.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1U685	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,

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Summary

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