Canonical Allele Identifier:
CA1365145666
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53057100C= , CM000665.2:g.53057100C= | GRCh38 |
| NC_000003.11:g.53091116C= , CM000665.1:g.53091116C= | GRCh37 |
| NC_000003.10:g.53066156C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607203.1:c.318-9861G= | ||
| ENST00000607283.5:c.465-13846G= | ||
| ENST00000607495.5:c.447+20588G= |