Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3322223826
- Species
- Rattus norvegicus
- Symbol
- rs3322223826
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Grk3
- Location
- 12:43650992
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)12:43650992C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000082322.2:c.114-4636C>T
- ENSEMBL:ENSRNOT00000082593.2:c.114-4636C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:43624778...43735375 (110.60 kb)
- Assembly version
- Not Available
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