Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90501197A= , CM000677.2:g.90501197A= | GRCh38 |
| NC_000015.9:g.91044429A= , CM000677.1:g.91044429A= | GRCh37 |
| NC_000015.8:g.88845433A= | NCBI36 |
| NG_052946.1:g.117957A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268182.10:c.*1089A= MANE Select | ENSP00000268182.5:n.*1089A= | |
| ENST00000268182.9:c.*1089A= | ENSP00000268182.5:n.*1089A= | |
| ENST00000558957.1:n.2121A= | ||
| ENST00000561086.1:n.1830A= | ||
| NM_003870.3:c.*1089A= | NP_003861.1:n.*1089A= | |
| XR_001751409.2:n.6192A= | ||
| NM_003870.4:c.*1089A= MANE Select | NP_003861.1:n.*1089A= |