Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323179701
- Species
- Rattus norvegicus
- Symbol
- rs3323179701
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gmds
- Location
- 17:32130542
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)17:32130542T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000023691.6:c.102+34903T>C
- ENSEMBL:ENSRNOT00000104164.1:c.102+34903T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:32095315...32621975 (526.66 kb)
- Assembly version
- Not Available
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