Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71030647T= , CM000666.2:g.71030647T= | GRCh38 |
| NC_000004.11:g.71896364T= , CM000666.1:g.71896364T= | GRCh37 |
| NC_000004.10:g.72115228T= | NCBI36 |
| NG_023303.1:g.42100T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286648.10:c.*1269T= MANE Select | ENSP00000286648.5:n.*1269T= | |
| ENST00000286648.9:c.*1269T= | ENSP00000286648.5:n.*1269T= | |
| ENST00000503359.5:c.*1996T= | ENSP00000426389.1:n.*1996T= | |
| ENST00000504730.5:c.*1336T= | ENSP00000425578.1:n.*1336T= | |
| ENST00000504952.1:c.*1195T= | ENSP00000421508.1:n.*1195T= | |
| NM_000788.2:c.*1269T= | NP_000779.1:n.*1269T= | |
| NM_000788.3:c.*1269T= MANE Select | NP_000779.1:n.*1269T= |