Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs770774345
- Species
- Homo sapiens
- Symbol
- rs770774345
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CLEC3B
- Location
- 3:45035919
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- NC_000003.12:g.45035919G>A
- HGVS.c name
- ENSEMBL:ENST00000296130.5:c.604G>A
- ENSEMBL:ENST00000428034.1:c.478G>A
- HGVS.p name
- ENSP00000296130:p.Val202Met
- ENSP00000396013:p.Val160Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:45001548...45036071 (34.52 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction