Canonical Allele Identifier:
CA2000590025
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112164844T= , CM000673.2:g.112164844T= | GRCh38 |
| NC_000011.9:g.112035567T= , CM000673.1:g.112035567T= | GRCh37 |
| NC_000011.8:g.111540777T= | NCBI36 |
| NG_028143.1:g.4274A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525987.5:n.320-5575T= | ||
| ENST00000531744.5:c.315-5575T= | ENSP00000456957.1:n.315-5575T= | |
| ENST00000532699.1:c.315-5575T= | ENSP00000456434.1:n.315-5575T= |