Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs750088430
- Species
- Homo sapiens
- Symbol
- rs750088430
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IL17RB
- Location
- 3:53860142
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)3:53860142C>T
- HGVS.c name
- ENSEMBL:ENST00000288167.8:c.860C>T
- ENSEMBL:ENST00000475124.1:n.1893C>T
- HGVS.p name
- ENSP00000288167:p.Pro287Leu
- ENSP00000418638:p.Pro271Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:53846568...53865794 (19.23 kb)
- Assembly version
- Not Available
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