HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151870A= , CM000681.2:g.55151870A= | GRCh38 |
NC_000019.9:g.55663238A= , CM000681.1:g.55663238A= | GRCh37 |
NC_000019.8:g.60355050A= | NCBI36 |
NG_007866.2:g.10863T= , LRG_432:g.10863T= | |
NG_011829.2:g.2369T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.597T= MANE Select | ENSP00000341838.5:p.Ser199= | |
ENST00000665070.1:c.630T= | ENSP00000499482.1:p.Ser210= | |
ENST00000344887.9:c.597T= | ENSP00000341838.5:p.Ser199= | |
ENST00000585806.5:n.596T= | ||
ENST00000588882.1:c.522T= | ENSP00000466729.1:p.Ser174= | |
ENST00000589864.1:n.425T= | ||
NM_000363.4:c.597T= , LRG_432t1:c.597T= | NP_000354.4:p.Ser199= | |
NM_000363.5:c.597T= MANE Select | NP_000354.4:p.Ser199= |