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

Gene: RNASEH2B ENSCHOG00000013688

Description

ribonuclease H2 subunit B [Source:HGNC Symbol;Acc:HGNC:25671]

Location

About this gene

This gene has 1 transcript (splice variant) and 223 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSCHOT00000013729.1	RNASEH2B-201	927	308aa	ENSCHOP00000012114.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,

Summary