Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778066242
- Species
- Homo sapiens
- Symbol
- rs778066242
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AP2S1
- Location
- 19:46839597
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000019.10:g.46839597G>A
- HGVS.c name
- ENSEMBL:ENST00000263270.11:c.154-19C>T
- ENSEMBL:ENST00000352203.8:c.177C>T
- HGVS.p name
- ENSP00000263271:p.Asp59=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:46838136...46850846 (12.71 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction