Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs41281465
- Species
- Homo sapiens
- Symbol
- rs41281465
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRKCE
- Location
- 2:46007502
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.46007502A>G
- HGVS.c name
- ENSEMBL:ENST00000306156.8:c.1104A>G
- ENSEMBL:ENST00000394874.1:c.273A>G
- HGVS.p name
- ENSP00000306124:p.Ser368=
- ENSP00000378341:p.Ser91=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:45651279...46187990 (536.71 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction