Canonical Allele Identifier:
CA1365145669
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53057105G= , CM000665.2:g.53057105G= | GRCh38 |
| NC_000003.11:g.53091121G= , CM000665.1:g.53091121G= | GRCh37 |
| NC_000003.10:g.53066161G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607203.1:c.318-9866C= | ||
| ENST00000607283.5:c.465-13851C= | ||
| ENST00000607495.5:c.447+20583C= |