Canonical Allele Identifier:
CA1608913571
Gene:
Linked Data
dbSNP Id:
rs1759189266
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.8169377C>A , CM000668.2:g.8169377C>A | GRCh38 |
| NC_000006.11:g.8169610C>A , CM000668.1:g.8169610C>A | GRCh37 |
| NC_000006.10:g.8114609C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926440.1:n.82+11117C>A | ||
| XR_926441.1:n.189+1457C>A | ||
| XR_926442.1:n.82+11117C>A | ||
| XR_926443.1:n.82+11117C>A | ||
| XR_001743950.1:n.179+1457C>A | ||
| XR_926440.2:n.74+11117C>A | ||
| XR_926441.2:n.179+1457C>A | ||
| XR_926443.2:n.83+11117C>A |