Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs239329432
- Species
- Mus musculus
- Symbol
- rs239329432
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Celf5
- Location
- 10:81317009
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)10:81317009T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000118763.1:c.145+1286A>G
- ENSEMBL:ENSMUST00000120508.1:c.145+1286A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:81295061...81318543 (23.48 kb)
- Assembly version
- Not Available
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