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