Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs979365377
- Species
- Homo sapiens
- Symbol
- rs979365377
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LARGE1
- Location
- 22:33304472
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)22:33304472T>C
- HGVS.c name
- ENSEMBL:ENST00000354992.7:c.1487A>G
- ENSEMBL:ENST00000397394.8:c.1487A>G
- HGVS.p name
- ENSP00000347088:p.Glu496Gly
- ENSP00000380549:p.Glu496Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:33066663...33922841 (856.18 kb)
- Assembly version
- Not Available
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