Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs32008319
- Species
- Mus musculus
- Symbol
- rs32008319
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lin9
- Location
- 1:180470865
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)1:180470865C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000192561.1:c.31+1903C>T
- ENSEMBL:ENSMUST00000192725.1:c.31+1903C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:180468715...180518252 (49.54 kb)
- Assembly version
- Not Available
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