Canonical Allele Identifier:
CA1689218047
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.13400547A= , CM000669.2:g.13400547A= | GRCh38 |
| NC_000007.13:g.13440172A= , CM000669.1:g.13440172A= | GRCh37 |
| NC_000007.12:g.13406697A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745097.1:n.147+90224A= |