Canonical Allele Identifier:
CA2059285111
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102501585A= , CM000674.2:g.102501585A= | GRCh38 |
| NC_000012.11:g.102895363A= , CM000674.1:g.102895363A= | GRCh37 |
| NC_000012.10:g.101419493A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001749289.1:n.1952+17697A= |