Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs147492156
- Species
- Homo sapiens
- Symbol
- rs147492156
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ATRAID
- Location
- 2:27215499
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:27215499G>A
- HGVS.c name
- ENSEMBL:ENST00000380171.9:c.319G>A
- ENSEMBL:ENST00000405489.7:c.145G>A
- HGVS.p name
- ENSP00000369518:p.Gly107Ser
- ENSP00000384033:p.Gly49Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:27212041...27217183 (5.14 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction