Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs217211738
- Species
- Mus musculus
- Symbol
- rs217211738
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f8
- Location
- 7:48529964
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:48529964G>T
- HGVS.c name
- ENSEMBL:ENSMUST00000058745.1:c.15+62C>A
- ENSEMBL:ENSMUST00000119223.1:c.15+62C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:48516177...48531344 (15.17 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction