Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs375545024
- Species
- Homo sapiens
- Symbol
- rs375545024
- Category
- Variant
- Variant type
- SNP
- Overlaps
- METTL16
- Location
- 17:2420142
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.2420142C>T
- HGVS.c name
- ENSEMBL:ENST00000263092.11:c.1517G>A
- ENSEMBL:ENST00000571669.6:n.1522G>A
- HGVS.p name
- ENSP00000263092:p.Arg506His
- NP_076991:p.Arg506His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:2405562...2511891 (106.33 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction