Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319443739
- Species
- Rattus norvegicus
- Symbol
- rs3319443739
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Retreg1
- Location
- 2:76447369
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)2:76447369A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000063951.4:c.408-17789A>T
- ENSEMBL:ENSRNOT00000079455.2:c.35+5211A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:76335609...76493898 (158.29 kb)
- Assembly version
- Not Available
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