HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151788T= , CM000681.2:g.55151788T= | GRCh38 |
NC_000019.9:g.55663156T= , CM000681.1:g.55663156T= | GRCh37 |
NC_000019.8:g.60354968T= | NCBI36 |
NG_007866.2:g.10945A= , LRG_432:g.10945A= | |
NG_011829.2:g.2451A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.*46A= MANE Select | ENSP00000341838.5:n.*46A= | |
ENST00000665070.1:c.*46A= | ENSP00000499482.1:n.*46A= | |
ENST00000344887.9:c.*46A= | ENSP00000341838.5:n.*46A= | |
ENST00000585806.5:n.678A= | ||
ENST00000588882.1:c.*46A= | ENSP00000466729.1:n.*46A= | |
ENST00000589864.1:n.507A= | ||
NM_000363.4:c.*46A= , LRG_432t1:c.*46A= | NP_000354.4:n.*46A= | |
NM_000363.5:c.*46A= MANE Select | NP_000354.4:n.*46A= |