Canonical Allele Identifier:
CA1596629136
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.162656561G= , CM000667.2:g.162656561G= | GRCh38 |
| NC_000005.9:g.162083567G= , CM000667.1:g.162083567G= | GRCh37 |
| NC_000005.8:g.162016145G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001742958.1:n.418+3541C= |