Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105138441
- Species
- Rattus norvegicus
- Symbol
- rs105138441
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Katnal2
- Location
- 18:70595966
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051353.1:g.70595966A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000048702.7:c.51+11789T>C
- ENSEMBL:ENSRNOT00000117058.1:c.51+11789T>C
- 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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