Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs217672700
- Species
- Mus musculus
- Symbol
- rs217672700
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Grm2
- Location
- 9:106528169
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCm39)9:106528169C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000023959.1:c.714G>A
- ENSEMBL:ENSMUST00000201681.1:c.714G>A
- HGVS.p name
- ENSEMBL:ENSMUSP00000023959:p.Ser238=
- ENSEMBL:ENSMUSP00000144631:p.Ser238=
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction