Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs226761492
- Species
- Mus musculus
- Symbol
- rs226761492
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Med12l
- Location
- 3:59041264
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)3:59041264G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000040325.1:c.2145+40148G>A
- ENSEMBL:ENSMUST00000164225.1:c.2250+40148G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:58913246...59226103 (312.86 kb)
- Assembly version
- Not Available
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