Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1567732054
- Species
- Homo sapiens
- Symbol
- rs1567732054
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC16A13
- Location
- 17:7036820
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.7036820C>G
- HGVS.c name
- ENSEMBL:ENST00000308027.7:c.293C>G
- ENSEMBL:ENST00000575844.1:n.724C>G
- HGVS.p name
- ENSP00000309751:p.Ser98Cys
- NP_963860:p.Ser98Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:7036015...7040117 (4.10 kb)
- Assembly version
- Not Available
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