Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs216912468
- Species
- Mus musculus
- Symbol
- rs216912468
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tcf20
- Location
- 15:82767605
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)15:82767605A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000048966.1:c.-36-26120T>G
- ENSEMBL:ENSMUST00000109510.1:c.-36-26120T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:82692637...82872073 (179.44 kb)
- Assembly version
- Not Available
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