HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154188T= , CM000681.2:g.55154188T= | GRCh38 |
NC_000019.9:g.55665556T= , CM000681.1:g.55665556T= | GRCh37 |
NC_000019.8:g.60357368T= | NCBI36 |
NG_007866.2:g.8545A= , LRG_432:g.8545A= | |
NG_011829.2:g.51A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.391A= MANE Select | ENSP00000341838.5:p.Lys131= | |
ENST00000665070.1:c.424A= | ENSP00000499482.1:p.Lys142= | |
ENST00000344887.9:c.391A= | ENSP00000341838.5:p.Lys131= | |
ENST00000585806.5:n.390A= | ||
ENST00000586669.5:n.399A= | ||
ENST00000588882.1:c.316A= | ENSP00000466729.1:p.Lys106= | |
ENST00000589864.1:n.219A= | ||
NM_000363.4:c.391A= , LRG_432t1:c.391A= | NP_000354.4:p.Lys131= | |
NM_000363.5:c.391A= MANE Select | NP_000354.4:p.Lys131= |