Canonical Allele Identifier:
CA2206404131
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9249413C= , CM000678.2:g.9249413C= | GRCh38 |
| NC_000016.9:g.9343270C= , CM000678.1:g.9343270C= | GRCh37 |
| NC_000016.8:g.9250771C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_933054.1:n.70+64680C= |