Canonical Allele Identifier:
CA2199721364
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.99817304A= , CM000677.2:g.99817304A= | GRCh38 |
| NC_000015.9:g.100357509A= , CM000677.1:g.100357509A= | GRCh37 |
| NC_000015.8:g.98175032A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932717.1:n.408+4218A= | ||
| XR_932718.1:n.408+4218A= | ||
| XR_932719.1:n.514+9002A= | ||
| XR_932720.1:n.409-1634A= | ||
| NR_135737.1:n.346+4218A= |