HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151898T= , CM000681.2:g.55151898T= | GRCh38 |
NC_000019.9:g.55663266T= , CM000681.1:g.55663266T= | GRCh37 |
NC_000019.8:g.60355078T= | NCBI36 |
NG_007866.2:g.10835A= , LRG_432:g.10835A= | |
NG_011829.2:g.2341A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.569A= MANE Select | ENSP00000341838.5:p.Asp190= | |
ENST00000665070.1:c.602A= | ENSP00000499482.1:p.Asp201= | |
ENST00000344887.9:c.569A= | ENSP00000341838.5:p.Asp190= | |
ENST00000585806.5:n.568A= | ||
ENST00000588882.1:c.494A= | ENSP00000466729.1:p.Asp165= | |
ENST00000589864.1:n.397A= | ||
NM_000363.4:c.569A= , LRG_432t1:c.569A= | NP_000354.4:p.Asp190= | |
NM_000363.5:c.569A= MANE Select | NP_000354.4:p.Asp190= |