Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319821544
- Species
- Rattus norvegicus
- Symbol
- rs3319821544
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Or1j13c
- Location
- 3:20315220
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)3:20315220G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000045825.2:c.59G>A
- RefSeq:NM_001000384.1:c.59G>A
- HGVS.p name
- ENSRNOP00000049367:p.Arg20Gln
- NP_001000384:p.Arg20Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:20315162...20316100 (0.94 kb)
- Assembly version
- Not Available
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