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: HBB ENSPTRG00000040047

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Description

hemoglobin subunit beta [Source:VGNC Symbol;Acc:VGNC:3255]

Location

Chromosome 11: 4,980,274-4,982,001 reverse strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 1 transcript (splice variant), 520 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000006177.4	HBB-201	748	147aa	ENSPTRP00000005700.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8P6S4 A0A663DJ46 P68873	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,

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Summary

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