Canonical Allele Identifier:
CA2298481281
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.41477771C= , CM000680.2:g.41477771C= | GRCh38 |
| NC_000018.9:g.39057735C= , CM000680.1:g.39057735C= | GRCh37 |
| NC_000018.8:g.37311733C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_935409.1:n.86-26363C= |