Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2146164178
- Species
- Homo sapiens
- Symbol
- rs2146164178
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LARGE1
- Location
- 22:33304342
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)22:33304342C>T
- HGVS.c name
- ENSEMBL:ENST00000354992.7:c.1617G>A
- ENSEMBL:ENST00000397394.8:c.1617G>A
- HGVS.p name
- ENSP00000347088:p.Gln539=
- ENSP00000380549:p.Gln539=
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction