Canonical Allele Identifier:
CA2025019717
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.29951209T= , CM000674.2:g.29951209T= | GRCh38 |
| NC_000012.11:g.30104142T= , CM000674.1:g.30104142T= | GRCh37 |
| NC_000012.10:g.29995409T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001749060.1:n.314-8169A= | |
| XR_001749061.1:n.314-8169A= | |
| XR_931473.1:n.314-8169A= | |
| XR_931474.1:n.314-8169A= | |
| XR_931475.1:n.135-8169A= |