Canonical Allele Identifier:
CA2065113657
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.115439972T= , CM000674.2:g.115439972T= | GRCh38 |
| NC_000012.11:g.115877777T= , CM000674.1:g.115877777T= | GRCh37 |
| NC_000012.10:g.114362160T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_945388.1:n.461-32641A= | |
| XR_945388.2:n.465-32641A= | |
| XR_945389.1:n.461-32641A= | |
| XR_945389.2:n.465-32641A= |