Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323292317
- Species
- Rattus norvegicus
- Symbol
- rs3323292317
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pura
- Location
- 18:27891111
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- NC_051353.1:g.27891111C>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000094968.1:c.77C>A
- ENSEMBL:ENSRNOT00000098397.1:c.77C>A
- HGVS.p name
- ENSRNOP00000076624:p.Ser26Ter
- ENSRNOP00000080018:p.Ser26Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:27884556...27905513 (20.96 kb)
- Assembly version
- Not Available
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