Canonical Allele Identifier:
CA1458374948
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.53933078T= , CM000666.2:g.53933078T= | GRCh38 |
| NC_000004.11:g.54799245T= , CM000666.1:g.54799245T= | GRCh37 |
| NC_000004.10:g.54494002T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507166.5:c.1018-341847T= | ENSP00000423325.1:n.1018-341847T= |