Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs782717759
- Species
- Homo sapiens
- Symbol
- rs782717759
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HSPB2
- Location
- 11:111913650
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (GRCh38)11:111913650C>T
- HGVS.c name
- ENSEMBL:ENST00000304298.4:c.304C>T
- ENSEMBL:ENST00000527616.1:n.398C>T
- HGVS.p name
- ENSP00000302476:p.Arg102Trp
- NP_001532:p.Arg102Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:111912734...111914093 (1.36 kb)
- Assembly version
- Not Available
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