Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs377644327
- Species
- Homo sapiens
- Symbol
- rs377644327
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EVI5
- Location
- 1:92624305
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:92624305C>G
- HGVS.c name
- ENSEMBL:ENST00000370331.5:c.1650G>C
- ENSEMBL:ENST00000468580.5:n.413G>C
- HGVS.p name
- ENSP00000359356:p.Trp550Cys
- ENSP00000440826:p.Trp561Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:92508696...92792410 (283.71 kb)
- Assembly version
- Not Available
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