Canonical Allele Identifier:
CA1827744262
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.1787481T= , CM000671.2:g.1787481T= | GRCh38 |
| NC_000009.11:g.1787481T= , CM000671.1:g.1787481T= | GRCh37 |
| NC_000009.10:g.1777481T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001746599.1:n.142+68569T= |