Canonical Allele Identifier:
CA1888360489
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.6747501C= , CM000672.2:g.6747501C= | GRCh38 |
| NC_000010.10:g.6789463C= , CM000672.1:g.6789463C= | GRCh37 |
| NC_000010.9:g.6829469C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930621.1:n.314-1438G= |