Canonical Allele Identifier:
CA2284239326
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.10321220C= , CM000680.2:g.10321220C= | GRCh38 |
| NC_000018.9:g.10321217C= , CM000680.1:g.10321217C= | GRCh37 |
| NC_000018.8:g.10311217C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935138.1:n.665+928G= | ||
| XR_001753344.1:n.650+928G= | ||
| XR_001753345.1:n.901G= | ||
| XR_001753346.1:n.549+928G= |