Canonical Allele Identifier:
CA1596629141
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.162656565G= , CM000667.2:g.162656565G= | GRCh38 |
| NC_000005.9:g.162083571G= , CM000667.1:g.162083571G= | GRCh37 |
| NC_000005.8:g.162016149G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001742958.1:n.418+3537C= |