Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs184267301
- Species
- Homo sapiens
- Symbol
- rs184267301
- Category
- Variant
- Variant type
- SNP
- Overlaps
- METTL16
- Location
- 17:2420170
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:2420170C>T
- HGVS.c name
- ENSEMBL:ENST00000263092.11:c.1489G>A
- ENSEMBL:ENST00000571669.6:n.1494G>A
- HGVS.p name
- ENSP00000263092:p.Gly497Ser
- NP_076991:p.Gly497Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:2405562...2511891 (106.33 kb)
- Assembly version
- Not Available
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