Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766037809
- Species
- Homo sapiens
- Symbol
- rs766037809
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RBM14
- Location
- 11:66624934
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000011.10:g.66624934C>T
- HGVS.c name
- ENSEMBL:ENST00000310137.5:c.1058C>T
- ENSEMBL:ENST00000393979.3:c.448+610C>T
- HGVS.p name
- ENSP00000311747:p.Ala353Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:66616626...66629934 (13.31 kb)
- Assembly version
- Not Available
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