Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs371378644
- Species
- Homo sapiens
- Symbol
- rs371378644
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC7A5
- Location
- 16:87836492
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- NC_000016.10:g.87836492G>T
- HGVS.c name
- ENSEMBL:ENST00000261622.5:c.1290+6C>A
- ENSEMBL:ENST00000563489.1:n.308+6C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:87830016...87869507 (39.49 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction