Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs768586669
- Species
- Homo sapiens
- Symbol
- rs768586669
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ALDH6A1
- Location
- 14:74084356
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)14:74084356C>T
- HGVS.c name
- ENSEMBL:ENST00000350259.8:c.39G>A
- ENSEMBL:ENST00000553458.6:c.39G>A
- HGVS.p name
- ENSP00000342564:p.Arg13=
- ENSP00000450436:p.Arg13=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:74056847...74084492 (27.65 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction