Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs226687066
- Species
- Mus musculus
- Symbol
- rs226687066
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Commd2
- Location
- 3:57554339
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)3:57554339T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000041954.1:c.*167-42A>G
- ENSEMBL:ENSMUST00000160959.1:c.403-42A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:57551770...57559105 (7.34 kb)
- Assembly version
- Not Available
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