Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs770316787
- Species
- Homo sapiens
- Symbol
- rs770316787
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EVI5
- Location
- 1:92607606
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:92607606C>T
- HGVS.c name
- ENSEMBL:ENST00000370331.5:c.1901G>A
- ENSEMBL:ENST00000491940.5:c.754G>A
- HGVS.p name
- ENSP00000359356:p.Arg634His
- ENSP00000440826:p.Arg645His
- 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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