Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs747405056
- Species
- Homo sapiens
- Symbol
- rs747405056
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RIPOR3
- Location
- 20:50596151
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)20:50596151C>G
- HGVS.c name
- ENSEMBL:ENST00000045083.6:c.1891G>C
- ENSEMBL:ENST00000327979.8:c.1903G>C
- HGVS.p name
- ENSP00000045083:p.Ala631Pro
- ENSP00000332663:p.Ala635Pro
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:50586108...50691542 (105.43 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction