HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154028A= , CM000681.2:g.55154028A= | GRCh38 |
NC_000019.9:g.55665396A= , CM000681.1:g.55665396A= | GRCh37 |
NC_000019.8:g.60357208A= | NCBI36 |
NG_007866.2:g.8705T= , LRG_432:g.8705T= | |
NG_011829.2:g.211T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.549+2T= MANE Select | ENSP00000341838.5:n.549+2T= | |
ENST00000665070.1:c.582+2T= | ENSP00000499482.1:n.582+2T= | |
ENST00000344887.9:c.549+2T= | ENSP00000341838.5:n.549+2T= | |
ENST00000585806.5:n.548+2T= | ||
ENST00000588882.1:c.474+2T= | ENSP00000466729.1:n.474+2T= | |
ENST00000589864.1:n.377+2T= | ||
NM_000363.4:c.549+2T= , LRG_432t1:c.549+2T= | NP_000354.4:n.549+2T= | |
NM_000363.5:c.549+2T= MANE Select | NP_000354.4:n.549+2T= |