Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323313252
- Species
- Rattus norvegicus
- Symbol
- rs3323313252
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Slc7a5
- Location
- 19:49962246
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)19:49962246C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000025784.3:c.541+974G>A
- RefSeq:NM_017353.2:c.541+974G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:49935220...49963823 (28.60 kb)
- Assembly version
- Not Available
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