Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2143738378
- Species
- Homo sapiens
- Symbol
- rs2143738378
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC7A5
- Location
- 16:87841083
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:87841083G>A
- HGVS.c name
- ENSEMBL:ENST00000261622.5:c.737C>T
- ENSEMBL:ENST00000565644.6:c.-62C>T
- HGVS.p name
- ENSP00000261622:p.Ala246Val
- NP_003477:p.Ala246Val
- 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