Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs773974453
- Species
- Homo sapiens
- Symbol
- rs773974453
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLEKHG4B
- Location
- 5:143421
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.143421A>G
- HGVS.c name
- ENSEMBL:ENST00000283426.11:c.661A>G
- ENSEMBL:ENST00000502646.1:c.403A>G
- HGVS.p name
- ENSP00000283426:p.Thr221Ala
- ENSP00000422493:p.Thr135Ala
- 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