Canonical Allele Identifier:
CA1480021898
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99474190_99474191delinsAT , CM000666.2:g.99474190_99474191delinsAT | GRCh38 |
| NC_000004.11:g.100395347_100395348delinsAT , CM000666.1:g.100395347_100395348delinsAT | GRCh37 |
| NC_000004.10:g.100614370_100614371delinsAT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000506494.1:n.243-2329_243-2328delinsAT |