Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1344384758
- Species
- Homo sapiens
- Symbol
- rs1344384758
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DYNC2I2
- Location
- 9:128634804
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:128634804C>T
- HGVS.c name
- ENSEMBL:ENST00000372715.7:c.1099G>A
- ENSEMBL:ENST00000483181.1:n.692G>A
- HGVS.p name
- ENSP00000361800:p.Gly367Arg
- NP_443076:p.Gly367Arg
- 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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