Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs765290273
- Species
- Homo sapiens
- Symbol
- rs765290273
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CAPNS1
- Location
- 19:36142712
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:36142712C>T
- HGVS.c name
- ENSEMBL:ENST00000246533.8:c.304C>T
- ENSEMBL:ENST00000586851.5:c.137C>T
- HGVS.p name
- ENSP00000246533:p.Arg102Trp
- ENSP00000464849:p.Arg102Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:36139953...36150353 (10.40 kb)
- Assembly version
- Not Available
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