Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200413853
- Species
- Homo sapiens
- Symbol
- rs200413853
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARMC8
- Location
- 3:138228964
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.138228964G>A
- HGVS.c name
- ENSEMBL:ENST00000358441.6:c.440G>A
- ENSEMBL:ENST00000461600.5:c.482G>A
- HGVS.p name
- ENSP00000351221:p.Arg147His
- ENSP00000417304:p.Arg119His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:138187248...138298389 (111.14 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction