Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.111754860A= , CM000663.2:g.111754860A= | GRCh38 |
| NC_000001.10:g.112297482A= , CM000663.1:g.112297482A= | GRCh37 |
| NC_000001.9:g.112099005A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679724.1:c.-64A= (DDX20) | ENSP00000505857.1:n.-64A= | |
| ENST00000412270.1:n.222+428T= (INKA2) | ||
| ENST00000444059.2:c.12+841T= (INKA2) | ENSP00000408238.2:n.12+841T= | |
| ENST00000625113.1:n.678T= (INKA2) | ||
| NM_198926.2:c.12+841T= (INKA2) | NP_945120.1:n.12+841T= | |
| NR_125963.1:n.222+428T= |