Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3321369508
- Species
- Rattus norvegicus
- Symbol
- rs3321369508
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Arcn1
- Location
- 8:45057978
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)8:45057978C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000082687.2:c.*1442G>A
- ENSEMBL:ENSRNOT00000102084.1:c.*1363G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:45057617...45082247 (24.63 kb)
- Assembly version
- Not Available
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