HGVS | Genome Assembly |
---|---|
NC_000004.12:g.71030713T= , CM000666.2:g.71030713T= | GRCh38 |
NC_000004.11:g.71896430T= , CM000666.1:g.71896430T= | GRCh37 |
NC_000004.10:g.72115294T= | NCBI36 |
NG_023303.1:g.42166T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286648.10:c.*1335T= MANE Select | ENSP00000286648.5:n.*1335T= | |
ENST00000286648.9:c.*1335T= | ENSP00000286648.5:n.*1335T= | |
ENST00000503359.5:c.*2062T= | ENSP00000426389.1:n.*2062T= | |
ENST00000504730.5:c.*1402T= | ENSP00000425578.1:n.*1402T= | |
ENST00000504952.1:c.*1261T= | ENSP00000421508.1:n.*1261T= | |
NM_000788.2:c.*1335T= | NP_000779.1:n.*1335T= | |
NM_000788.3:c.*1335T= MANE Select | NP_000779.1:n.*1335T= |