Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322004964
- Species
- Rattus norvegicus
- Symbol
- rs3322004964
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ENSRNOG00000063579
- Location
- 13:43645882
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)13:43645882A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000095513.1:n.1157A>C
- ENSEMBL:ENSRNOT00000097457.1:n.976A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:43631977...43650173 (18.20 kb)
- Assembly version
- Not Available
- Viewer Help
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