Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323153776
- Species
- Rattus norvegicus
- Symbol
- rs3323153776
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E230025N22Rikl
- Location
- 18:28291450
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051353.1:g.28291450T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000108010.1:c.466+96A>G
- RefSeq:NM_001402538.1:c.466+96A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:28285980...28295204 (9.22 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction