Canonical Allele Identifier:
CA2298481252
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.41477697C= , CM000680.2:g.41477697C= | GRCh38 |
| NC_000018.9:g.39057661C= , CM000680.1:g.39057661C= | GRCh37 |
| NC_000018.8:g.37311659C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935409.1:n.86-26437C= |