Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs228766243
- Species
- Mus musculus
- Symbol
- rs228766243
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gnaq
- Location
- 19:16113024
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)19:16113024C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000025541.1:c.136+2199C>T
- RefSeq:NM_008139.6:c.136+2199C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:16110195...16364827 (254.63 kb)
- Assembly version
- Not Available
- Viewer Help
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