HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154804A>T , CM000681.2:g.55154804A>T | GRCh38 |
NC_000019.9:g.55666172A>T , CM000681.1:g.55666172A>T | GRCh37 |
NC_000019.8:g.60357984A>T | NCBI36 |
NG_007866.2:g.7929T>A , LRG_432:g.7929T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.309T>A MANE Select | ENSP00000341838.5:p.Arg103= | |
ENST00000665070.1:c.309T>A | ENSP00000499482.1:p.Arg103= | |
ENST00000344887.9:c.309T>A | ENSP00000341838.5:p.Arg103= | |
ENST00000585806.5:n.308T>A | ||
ENST00000586669.5:n.317T>A | ||
ENST00000587176.5:n.493T>A | ||
ENST00000587871.1:c.928T>A | ||
ENST00000588882.1:c.234T>A | ENSP00000466729.1:p.Arg78= | |
ENST00000590463.1:n.481T>A | ||
NM_000363.4:c.309T>A , LRG_432t1:c.309T>A | NP_000354.4:p.Arg103= | |
NM_000363.5:c.309T>A MANE Select | NP_000354.4:p.Arg103= |