Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1330666981
- Species
- Homo sapiens
- Symbol
- rs1330666981
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CYP1A1
- Location
- 15:74720586
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:74720586C>G
- HGVS.c name
- ENSEMBL:ENST00000379727.8:c.1442G>C
- ENSEMBL:ENST00000395049.8:c.1355G>C
- HGVS.p name
- ENSP00000369050:p.Ser481Thr
- ENSP00000378489:p.Ser452Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:74719542...74725536 (5.99 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction