Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323367541
- Species
- Rattus norvegicus
- Symbol
- rs3323367541
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lsm6
- Location
- 19:29107546
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)19:29107546C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000071471.3:n.174+1568C>T
- ENSEMBL:ENSRNOT00000102121.1:n.555-1482C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:29098214...29118682 (20.47 kb)
- Assembly version
- Not Available
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