Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201293315
- Species
- Homo sapiens
- Symbol
- rs201293315
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CXCL1
- Location
- 4:73869751
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.73869751C>G
- HGVS.c name
- ENSEMBL:ENST00000395761.4:c.183C>G
- ENSEMBL:ENST00000509101.1:n.261C>G
- HGVS.p name
- ENSP00000379110:p.Asn61Lys
- NP_001502:p.Asn61Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:73869393...73871308 (1.92 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction