Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1042820924
- Species
- Homo sapiens
- Symbol
- rs1042820924
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARHGEF33
- Location
- 2:38959926
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:38959926C>G
- HGVS.c name
- ENSEMBL:ENST00000398800.8:c.1621C>G
- ENSEMBL:ENST00000483305.1:n.364C>G
- HGVS.p name
- ENSP00000381780:p.Leu541Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:38889875...38975454 (85.58 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction