Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321628152
- Species
- Rattus norvegicus
- Symbol
- rs3321628152
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rev1
- Location
- 9:40292362
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)9:40292362C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000067197.3:c.1671-662G>A
- ENSEMBL:ENSRNOT00000109166.1:c.-89-70430G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:40278100...40351764 (73.66 kb)
- Assembly version
- Not Available
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