Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs213139686
- Species
- Mus musculus
- Symbol
- rs213139686
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gdnf
- Location
- 15:7844180
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)15:7844180C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000022744.1:c.62-890C>T
- RefSeq:NM_001301332.1:c.62-890C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:7840327...7867056 (26.73 kb)
- Assembly version
- Not Available
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