HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55152074A= , CM000681.2:g.55152074A= | GRCh38 |
NC_000019.9:g.55663442A= , CM000681.1:g.55663442A= | GRCh37 |
NC_000019.8:g.60355254A= | NCBI36 |
NG_007866.2:g.10659T= , LRG_432:g.10659T= | |
NG_011829.2:g.2165T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.550-157T= MANE Select | ENSP00000341838.5:n.550-157T= | |
ENST00000665070.1:c.583-157T= | ENSP00000499482.1:n.583-157T= | |
ENST00000344887.9:c.550-157T= | ENSP00000341838.5:n.550-157T= | |
ENST00000585806.5:n.549-157T= | ||
ENST00000588882.1:c.475-157T= | ENSP00000466729.1:n.475-157T= | |
ENST00000589864.1:n.378-157T= | ||
NM_000363.4:c.550-157T= , LRG_432t1:c.550-157T= | NP_000354.4:n.550-157T= | |
NM_000363.5:c.550-157T= MANE Select | NP_000354.4:n.550-157T= |