Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12720280T= , CM000674.2:g.12720280T= | GRCh38 |
| NC_000012.11:g.12873214T= , CM000674.1:g.12873214T= | GRCh37 |
| NC_000012.10:g.12764481T= | NCBI36 |
| NG_016341.1:g.7913T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000614874.2:c.*1334T= | ENSP00000507272.1:n.*1334T= | |
| ENST00000682620.1:n.1761-756T= | ||
| ENST00000684771.1:n.715-756T= | ||
| ENST00000228872.9:c.*9-756T= MANE Select | ENSP00000228872.4:n.*9-756T= | |
| ENST00000228872.8:c.*9-756T= | ENSP00000228872.4:n.*9-756T= | |
| ENST00000396340.1:c.476-785T= | ENSP00000379629.1:n.476-785T= | |
| ENST00000442489.1:c.324-756T= | ENSP00000407597.1:n.324-756T= | |
| ENST00000477087.1:n.285-756T= | ||
| NM_004064.4:c.*9-756T= | NP_004055.1:n.*9-756T= | |
| NM_004064.5:c.*9-756T= MANE Select | NP_004055.1:n.*9-756T= |