Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs116033653
- Species
- Homo sapiens
- Symbol
- rs116033653
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLEKHG4B
- Location
- 5:181629
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)5:181629T>C
- HGVS.c name
- ENSEMBL:ENST00000283426.11:c.3450T>C
- ENSEMBL:ENST00000504041.1:n.1533T>C
- HGVS.p name
- ENSP00000283426:p.Cys1150=
- ENSP00000490806:p.Cys1506=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:92168...189972 (97.80 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction