Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs769226967
- Species
- Homo sapiens
- Symbol
- rs769226967
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLMAP
- Location
- 3:57862093
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- (GRCh38)3:57862093A>G
- HGVS.c name
- ENSEMBL:ENST00000295951.7:c.966+7A>G
- ENSEMBL:ENST00000295952.7:c.966+7A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:57755450...57930013 (174.56 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction