Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs216830348
- Species
- Mus musculus
- Symbol
- rs216830348
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Grm2
- Location
- 9:106526650
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)9:106526650C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000023959.1:c.1288+945G>A
- ENSEMBL:ENSMUST00000201681.1:c.1288+945G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:106521733...106533308 (11.58 kb)
- Assembly version
- Not Available
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