Canonical Allele Identifier:
CA1963376089
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.34759489G= , CM000673.2:g.34759489G= | GRCh38 |
| NC_000011.9:g.34781036G= , CM000673.1:g.34781036G= | GRCh37 |
| NC_000011.8:g.34737612G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_428897.2:n.579+4882G= | ||
| XR_931188.1:n.693+4882G= | ||
| XR_931189.1:n.854+4882G= | ||
| XR_931190.1:n.639+4882G= | ||
| XR_931191.1:n.689+4882G= | ||
| XR_001748174.1:n.855+4882G= | ||
| XR_001748176.1:n.1016+4882G= | ||
| XR_002957246.1:n.639+4882G= |