Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323076740
- Species
- Rattus norvegicus
- Symbol
- rs3323076740
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Camk4
- Location
- 18:24771952
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)18:24771952T>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000027771.5:c.538+586T>A
- ENSEMBL:ENSRNOT00000078822.2:c.622+586T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:24582988...24811918 (228.93 kb)
- Assembly version
- Not Available
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