Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154386A= , CM000681.2:g.55154386A= | GRCh38 |
| NC_000019.9:g.55665754A= , CM000681.1:g.55665754A= | GRCh37 |
| NC_000019.8:g.60357566A= | NCBI36 |
| NG_007866.2:g.8347T= , LRG_432:g.8347T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.373-180T= MANE Select | ENSP00000341838.5:n.373-180T= | |
| ENST00000665070.1:c.406-180T= | ENSP00000499482.1:n.406-180T= | |
| ENST00000344887.9:c.373-180T= | ENSP00000341838.5:n.373-180T= | |
| ENST00000585806.5:n.372-180T= | ||
| ENST00000586669.5:n.381-180T= | ||
| ENST00000587176.5:n.911T= | ||
| ENST00000588882.1:c.298-180T= | ENSP00000466729.1:n.298-180T= | |
| ENST00000589864.1:n.21T= | ||
| NM_000363.4:c.373-180T= , LRG_432t1:c.373-180T= | NP_000354.4:n.373-180T= | |
| NM_000363.5:c.373-180T= MANE Select | NP_000354.4:n.373-180T= |