Canonical Allele Identifier:
CA2266849982
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56538256T= , CM000679.2:g.56538256T= | GRCh38 |
| NC_000017.10:g.54615617T= , CM000679.1:g.54615617T= | GRCh37 |
| NC_000017.9:g.51970616T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_002958121.1:n.245-422A= | |
| XR_934871.1:n.245-422A= | |
| XR_934872.1:n.245-422A= |