Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs778815719
- Species
- Homo sapiens
- Symbol
- rs778815719
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CCL14
- Location
- 17:35984345
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)17:35984345C>T
- HGVS.c name
- ENSEMBL:ENST00000614009.1:c.253G>A
- ENSEMBL:ENST00000618404.5:c.187G>A
- HGVS.p name
- ENSP00000479097:p.Gly79Arg
- ENSP00000481023:p.Gly63Arg
- 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
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