Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs534249990
- Species
- Homo sapiens
- Symbol
- rs534249990
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WDR83
- Location
- 19:12675569
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)19:12675569C>T
- HGVS.c name
- ENSEMBL:ENST00000418543.8:c.845C>T
- ENSEMBL:ENST00000425834.7:n.534C>T
- HGVS.p name
- ENSP00000402653:p.Ser282Leu
- NP_001093207:p.Ser282Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:12666802...12675832 (9.03 kb)
- Assembly version
- Not Available
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