Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs243811489
- Species
- Mus musculus
- Symbol
- rs243811489
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cpt1a
- Location
- 19:3372711
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)19:3372711C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000237938.1:c.-14+13C>T
- RefSeq:XM_011248602.4:c.62+235C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:3372334...3435733 (63.40 kb)
- Assembly version
- Not Available
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