Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105730878
- Species
- Rattus norvegicus
- Symbol
- rs105730878
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Katnal2
- Location
- 18:70544216
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)18:70544216T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000048702.7:c.1214+4680A>G
- ENSEMBL:ENSRNOT00000098783.1:c.428+4680A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:70531754...70608082 (76.33 kb)
- Assembly version
- Not Available
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