Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs754488103
- Species
- Homo sapiens
- Symbol
- rs754488103
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DYNC2I2
- Location
- 9:128635665
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:128635665A>G
- HGVS.c name
- ENSEMBL:ENST00000372715.7:c.806T>C
- ENSEMBL:ENST00000419989.2:n.651T>C
- HGVS.p name
- ENSP00000361800:p.Val269Ala
- NP_443076:p.Val269Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:128633653...128684460 (50.81 kb)
- Assembly version
- Not Available
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