HGVS | Genome Assembly |
---|---|
NC_000023.11:g.120626713C= , CM000685.2:g.120626713C= | GRCh38 |
NC_000023.10:g.119760568C= , CM000685.1:g.119760568C= | GRCh37 |
NC_000023.9:g.119644596C= | NCBI36 |
NG_016219.1:g.8438G= |
HGVS | Amino-acid Change |
---|---|
NM_001011551.3:c.454G= MANE Select | NP_001011551.1:p.Glu152= |
ENST00000304661.6:c.454G= MANE Select | ENSP00000304364.5:p.Glu152= |
NM_001011551.2:c.454G= | NP_001011551.1:p.Glu152= |
NM_152692.4:c.454G= | NP_689905.1:p.Glu152= |
NM_152692.5:c.454G= | NP_689905.1:p.Glu152= |
ENST00000304661.5:c.454G= | ENSP00000304364.5:p.Glu152= |
ENST00000371313.2:c.454G= | ENSP00000360363.2:p.Glu152= |