| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17285544A= , CM000669.2:g.17285544A= | GRCh38 |
| NC_000007.13:g.17325168A= , CM000669.1:g.17325168A= | GRCh37 |
| NC_000007.12:g.17291693A= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000642825.1:c.-202-10753A= | ENSP00000495987.1:n.-202-10753A= |
| XR_927069.1:n.567+699T= | |
| XR_927070.1:n.567+699T= | |
| XR_927071.1:n.567+699T= | |
| XR_927072.1:n.568+699T= | |
| XR_927073.2:n.711+699T= |