Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.22035352G>T , CM000663.2:g.22035352G>T | GRCh38 |
| NC_000001.10:g.22361845G>T , CM000663.1:g.22361845G>T | GRCh37 |
| NC_000001.9:g.22234432G>T | NCBI36 |
| NG_047042.3:g.14842G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695855.1:c.-51+9980G>T | ENSP00000512220.1:n.-51+9980G>T | |
| ENST00000695856.1:c.-51+9713G>T | ENSP00000512221.1:n.-51+9713G>T | |
| ENST00000648594.1:c.-51+9713G>T (CDC42) | ENSP00000497733.1:n.-51+9713G>T | |
| XR_947048.1:n.84-3485C>A | ||
| XR_002958282.1:n.141-3485C>A (CDC42-AS1) |