Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs949593584
- Species
- Homo sapiens
- Symbol
- rs949593584
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MYO5C
- Location
- 15:52261026
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:52261026C>G
- HGVS.c name
- ENSEMBL:ENST00000261839.12:c.1149G>C
- ENSEMBL:ENST00000541028.5:n.980G>C
- HGVS.p name
- ENSP00000261839:p.Glu383Asp
- NP_061198:p.Glu383Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:52192322...52295804 (103.48 kb)
- Assembly version
- Not Available
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