Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322853926
- Species
- Rattus norvegicus
- Symbol
- rs3322853926
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Slmap
- Location
- 16:1718050
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051351.1:g.1718050C>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000091513.2:c.687+208G>C
- ENSEMBL:ENSRNOT00000113231.1:c.687+208G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:1667205...1785200 (118.00 kb)
- Assembly version
- Not Available
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