Canonical Allele Identifier:
CA1689284602
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.13514165A= , CM000669.2:g.13514165A= | GRCh38 |
| NC_000007.13:g.13553790A= , CM000669.1:g.13553790A= | GRCh37 |
| NC_000007.12:g.13520315A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745097.1:n.148-188151A= |