Canonical Allele Identifier:
CA1381014980
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.86206522T= , CM000665.2:g.86206522T= | GRCh38 |
| NC_000003.11:g.86255672T= , CM000665.1:g.86255672T= | GRCh37 |
| NC_000003.10:g.86338362T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_427356.2:n.681-589A= | ||
| XR_941024.1:n.680+16182A= | ||
| XR_941025.1:n.599-589A= | ||
| XR_427356.4:n.715-589A= | ||
| XR_941024.2:n.682+16182A= | ||
| XR_941025.3:n.632-589A= |