Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs207461693
- Species
- Homo sapiens
- Symbol
- rs207461693
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRKCE
- Location
- 2:45692171
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)2:45692171C>T
- HGVS.c name
- ENSEMBL:ENST00000306156.8:c.348+39723C>T
- ENSEMBL:ENST00000421201.1:c.348+39723C>T
- HGVS.p name
- Not Available
- 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
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