HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154153G= , CM000681.2:g.55154153G= | GRCh38 |
NC_000019.9:g.55665521G= , CM000681.1:g.55665521G= | GRCh37 |
NC_000019.8:g.60357333G= | NCBI36 |
NG_007866.2:g.8580C= , LRG_432:g.8580C= | |
NG_011829.2:g.86C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.426C= MANE Select | ENSP00000341838.5:p.Pro142= | |
ENST00000665070.1:c.459C= | ENSP00000499482.1:p.Pro153= | |
ENST00000344887.9:c.426C= | ENSP00000341838.5:p.Pro142= | |
ENST00000585806.5:n.425C= | ||
ENST00000586669.5:n.434C= | ||
ENST00000588882.1:c.351C= | ENSP00000466729.1:p.Pro117= | |
ENST00000589864.1:n.254C= | ||
NM_000363.4:c.426C= , LRG_432t1:c.426C= | NP_000354.4:p.Pro142= | |
NM_000363.5:c.426C= MANE Select | NP_000354.4:p.Pro142= |