Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs375426166
- Species
- Homo sapiens
- Symbol
- rs375426166
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARHGEF33
- Location
- 2:38953238
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:38953238T>C
- HGVS.c name
- ENSEMBL:ENST00000398800.8:c.1130T>C
- ENSEMBL:ENST00000409978.7:c.1130T>C
- HGVS.p name
- ENSP00000381780:p.Leu377Pro
- ENSP00000387020:p.Leu377Pro
- 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
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