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

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Gene: CHGB ENSCAFG00845027687

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Description

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

Location

Primary_assembly 24: 16,319,975-16,333,580 reverse strand.

ROS_Cfam_1.0:CM025123.1

About this gene

This gene has 3 transcripts (splice variants), 122 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCAFT00845048856.1	CHGB-202	2704	669aa	ENSCAFP00845038329.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0P546 A0A8I3Q1Q3	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,
ENSCAFT00845048896.1	CHGB-203	3380	618aa	ENSCAFP00845038355.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I3PUG4	-
ENSCAFT00845048830.1	CHGB-201	2987	622aa	ENSCAFP00845038312.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0QR44 A0A8I3Q3A9	-

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Summary

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