HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55152165T= , CM000681.2:g.55152165T= | GRCh38 |
NC_000019.9:g.55663533T= , CM000681.1:g.55663533T= | GRCh37 |
NC_000019.8:g.60355345T= | NCBI36 |
NG_007866.2:g.10568A= , LRG_432:g.10568A= | |
NG_011829.2:g.2074A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.550-248A= MANE Select | ENSP00000341838.5:n.550-248A= | |
ENST00000665070.1:c.583-248A= | ENSP00000499482.1:n.583-248A= | |
ENST00000344887.9:c.550-248A= | ENSP00000341838.5:n.550-248A= | |
ENST00000585806.5:n.549-248A= | ||
ENST00000588882.1:c.475-248A= | ENSP00000466729.1:n.475-248A= | |
ENST00000589864.1:n.378-248A= | ||
NM_000363.4:c.550-248A= , LRG_432t1:c.550-248A= | NP_000354.4:n.550-248A= | |
NM_000363.5:c.550-248A= MANE Select | NP_000354.4:n.550-248A= |