Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323324041
- Species
- Rattus norvegicus
- Symbol
- rs3323324041
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E230025N22Rikl
- Location
- 18:28292462
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)18:28292462C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000108010.1:c.325G>A
- RefSeq:NM_001402538.1:c.325G>A
- HGVS.p name
- ENSRNOP00000085189:p.Glu109Lys
- NP_001389467:p.Glu109Lys
- 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
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