Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1057521643
- Species
- Homo sapiens
- Symbol
- rs1057521643
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COX20
- Location
- 1:244835676
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (GRCh38)1:244835676C>G
- HGVS.c name
- ENSEMBL:ENST00000366528.3:c.-39C>G
- ENSEMBL:ENST00000391839.6:n.21C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244835306...244845063 (9.76 kb)
- Assembly version
- Not Available
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