Canonical Allele Identifier:
CA3002196679
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762620dup , CM000672.2:g.94762620dup | GRCh38 |
| NC_000010.10:g.96522377dup , CM000672.1:g.96522377dup | GRCh37 |
| NC_000010.9:g.96512367dup | NCBI36 |
| NG_008384.2:g.4915dup | |
| NG_008384.3:g.4940dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464755.1:c.932-12438dup | ENSP00000483243.1:n.932-12438dup |