HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151871C= , CM000681.2:g.55151871C= | GRCh38 |
NC_000019.9:g.55663239C= , CM000681.1:g.55663239C= | GRCh37 |
NC_000019.8:g.60355051C= | NCBI36 |
NG_007866.2:g.10862G= , LRG_432:g.10862G= | |
NG_011829.2:g.2368G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.596G= MANE Select | ENSP00000341838.5:p.Ser199= | |
ENST00000665070.1:c.629G= | ENSP00000499482.1:p.Ser210= | |
ENST00000344887.9:c.596G= | ENSP00000341838.5:p.Ser199= | |
ENST00000585806.5:n.595G= | ||
ENST00000588882.1:c.521G= | ENSP00000466729.1:p.Ser174= | |
ENST00000589864.1:n.424G= | ||
NM_000363.4:c.596G= , LRG_432t1:c.596G= | NP_000354.4:p.Ser199= | |
NM_000363.5:c.596G= MANE Select | NP_000354.4:p.Ser199= |