Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs215199928
- Species
- Mus musculus
- Symbol
- rs215199928
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Or4c107
- Location
- 2:88788441
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)2:88788441C>A
- HGVS.c name
- ENSEMBL:ENSMUST00000215781.1:c.-268-103C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:88788812...88789747 (0.94 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction