Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs32689212
- Species
- Mus musculus
- Symbol
- rs32689212
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rere
- Location
- 4:150525688
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)4:150525688C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000105682.1:c.522+1763C>T
- ENSEMBL:ENSMUST00000131600.1:c.342+9638C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:150366103...150706423 (340.32 kb)
- Assembly version
- Not Available
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