Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs31818655
- Species
- Mus musculus
- Symbol
- rs31818655
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Clpb
- Location
- 7:101314389
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:101314389G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000001884.1:c.403+969G>A
- ENSEMBL:ENSMUST00000106998.1:c.403+969G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:101312958...101444667 (131.71 kb)
- Assembly version
- Not Available
- Viewer Help
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