Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs229051337
- Species
- Mus musculus
- Symbol
- rs229051337
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f2
- Location
- 4:135902906
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)4:135902906C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000061721.1:c.258+2557C>T
- RefSeq:NM_177733.7:c.258+2557C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:135899705...135923368 (23.66 kb)
- Assembly version
- Not Available
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