Canonical Allele Identifier:
CA1462694369
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.62558443A= , CM000666.2:g.62558443A= | GRCh38 |
| NC_000004.11:g.63424161A= , CM000666.1:g.63424161A= | GRCh37 |
| NC_000004.10:g.63106756A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938814.1:n.161-5401A= |