HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151910C= , CM000681.2:g.55151910C= | GRCh38 |
NC_000019.9:g.55663278C= , CM000681.1:g.55663278C= | GRCh37 |
NC_000019.8:g.60355090C= | NCBI36 |
NG_007866.2:g.10823G= , LRG_432:g.10823G= | |
NG_011829.2:g.2329G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.557G= MANE Select | ENSP00000341838.5:p.Arg186= | |
ENST00000665070.1:c.590G= | ENSP00000499482.1:p.Arg197= | |
ENST00000344887.9:c.557G= | ENSP00000341838.5:p.Arg186= | |
ENST00000585806.5:n.556G= | ||
ENST00000588882.1:c.482G= | ENSP00000466729.1:p.Arg161= | |
ENST00000589864.1:n.385G= | ||
NM_000363.4:c.557G= , LRG_432t1:c.557G= | NP_000354.4:p.Arg186= | |
NM_000363.5:c.557G= MANE Select | NP_000354.4:p.Arg186= |