Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs579408222
- Species
- Mus musculus
- Symbol
- rs579408222
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sptb
- Location
- 12:76755240
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000078.7:g.76755240T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000021458.1:c.-55+1469A>G
- ENSEMBL:ENSMUST00000166101.1:c.-55+1469A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:76627262...76757321 (130.06 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction