Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs769854730
- Species
- Homo sapiens
- Symbol
- rs769854730
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CCL14
- Location
- 17:35984449
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:35984449C>T
- HGVS.c name
- ENSEMBL:ENST00000614009.1:c.149G>A
- ENSEMBL:ENST00000618404.5:c.83G>A
- HGVS.p name
- ENSP00000479097:p.Gly44Glu
- ENSP00000481023:p.Gly28Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:35983288...35987004 (3.72 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction