Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320003036
- Species
- Rattus norvegicus
- Symbol
- rs3320003036
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rbbp9
- Location
- 3:131925758
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)3:131925758C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000010678.5:c.*897G>A
- RefSeq:NM_019219.3:c.*946G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:131925095...131939042 (13.95 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction