Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs12141433
- Species
- Homo sapiens
- Symbol
- rs12141433
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COX20
- Location
- 1:244836499
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)1:244836499G>C
- HGVS.c name
- ENSEMBL:ENST00000366528.3:c.57G>C
- ENSEMBL:ENST00000391839.6:n.101+743G>C
- HGVS.p name
- ENSP00000355486:p.Ser19=
- 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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