Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs245885169
- Species
- Mus musculus
- Symbol
- rs245885169
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Immp2l
- Location
- 12:41376652
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)12:41376652G>C
- HGVS.c name
- ENSEMBL:ENSMUST00000132121.1:c.239+215710G>C
- ENSEMBL:ENSMUST00000134965.1:c.239+215710G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:41074089...42002371 (928.28 kb)
- Assembly version
- Not Available
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