Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs8170877
- Species
- Rattus norvegicus
- Symbol
- rs8170877
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cmpk2
- Location
- 6:43083945
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)6:43083945G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000052003.6:c.*479G>A
- RefSeq:NM_001108017.1:c.*479G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:43073706...43085183 (11.48 kb)
- Assembly version
- Not Available
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