Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.58401742C= , CM000677.2:g.58401742C= | GRCh38 |
| NC_000015.9:g.58693941C= , CM000677.1:g.58693941C= | GRCh37 |
| NC_000015.8:g.56481233C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558239.5:c.-172+18229G= | ENSP00000453292.1:n.-172+18229G= | |
| ENST00000560863.5:n.415+18229G= | ||
| XR_429537.2:n.164+18229G= | ||
| XR_932289.1:n.165-16886G= | ||
| XR_001751556.2:n.216+18229G= | ||
| XR_001751557.2:n.216+18229G= | ||
| XR_001751558.2:n.216+18229G= | ||
| XR_001751559.2:n.216+18229G= | ||
| XR_001751560.2:n.216+18229G= | ||
| XR_001751563.2:n.216+18229G= | ||
| XR_001751565.2:n.217-13246G= | ||
| XR_429537.4:n.216+18229G= |