Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs768389321
- Species
- Homo sapiens
- Symbol
- rs768389321
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC25A18
- Location
- 22:17583450
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)22:17583450G>A
- HGVS.c name
- ENSEMBL:ENST00000327451.11:c.325G>A
- ENSEMBL:ENST00000399813.1:c.325G>A
- HGVS.p name
- ENSP00000329033:p.Gly109Arg
- ENSP00000382710:p.Gly109Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:17563450...17590995 (27.55 kb)
- Assembly version
- Not Available
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