Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs51601486
- Species
- Mus musculus
- Symbol
- rs51601486
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scrt2
- Location
- 2:151932735
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000068.8:g.151932735A>T
- HGVS.c name
- ENSEMBL:ENSMUST00000064061.1:c.134-2247A>T
- RefSeq:NM_001160410.2:c.134-2247A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:151923737...151937722 (13.99 kb)
- Assembly version
- Not Available
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