Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs266206311
- Species
- Mus musculus
- Symbol
- rs266206311
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Abcd2
- Location
- 15:91074400
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)15:91074400C>A
- HGVS.c name
- ENSEMBL:ENSMUST00000069511.1:c.939+473G>T
- RefSeq:NM_001358967.2:c.939+473G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:91030074...91076002 (45.93 kb)
- Assembly version
- Not Available
- Viewer Help
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