Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs6603979
- Species
- Homo sapiens
- Symbol
- rs6603979
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EVI5
- Location
- 1:92513797
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.92513797A>G
- HGVS.c name
- ENSEMBL:ENST00000370331.5:c.2292T>C
- ENSEMBL:ENST00000540033.3:c.2325T>C
- HGVS.p name
- ENSP00000359356:p.Gly764=
- ENSP00000440826:p.Gly775=
- 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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