Canonical Allele Identifier:
CA2059285012
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102501387G= , CM000674.2:g.102501387G= | GRCh38 |
| NC_000012.11:g.102895165G= , CM000674.1:g.102895165G= | GRCh37 |
| NC_000012.10:g.101419295G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001749289.1:n.1952+17499G= |