Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.22047131C>A , CM000663.2:g.22047131C>A | GRCh38 |
| NC_000001.10:g.22373624C>A , CM000663.1:g.22373624C>A | GRCh37 |
| NC_000001.9:g.22246211C>A | NCBI36 |
| NG_047042.3:g.26621C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695855.1:c.-51+21759C>A | ENSP00000512220.1:n.-51+21759C>A | |
| ENST00000695856.1:c.-51+21492C>A | ENSP00000512221.1:n.-51+21492C>A | |
| ENST00000648594.1:c.-51+21492C>A (CDC42) | ENSP00000497733.1:n.-51+21492C>A | |
| XR_947048.1:n.83+5656G>T | ||
| XR_002958282.1:n.140+5656G>T (CDC42-AS1) |