Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs265051348
- Species
- Mus musculus
- Symbol
- rs265051348
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ncbp1
- Location
- 4:46139491
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)4:46139491C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000030014.1:c.34+605C>T
- RefSeq:NM_001033201.4:c.34+605C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:46138732...46172403 (33.67 kb)
- Assembly version
- Not Available
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