Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200234866
- Species
- Homo sapiens
- Symbol
- rs200234866
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CXCL1
- Location
- 4:73869716
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:73869716C>A
- HGVS.c name
- ENSEMBL:ENST00000395761.4:c.148C>A
- ENSEMBL:ENST00000509101.1:n.226C>A
- HGVS.p name
- ENSP00000379110:p.Gln50Lys
- NP_001502:p.Gln50Lys
- 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
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