HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154765T= , CM000681.2:g.55154765T= | GRCh38 |
NC_000019.9:g.55666133T= , CM000681.1:g.55666133T= | GRCh37 |
NC_000019.8:g.60357945T= | NCBI36 |
NG_007866.2:g.7968A= , LRG_432:g.7968A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.348A= MANE Select | ENSP00000341838.5:p.Ala116= | |
ENST00000665070.1:c.348A= | ENSP00000499482.1:p.Ala116= | |
ENST00000344887.9:c.348A= | ENSP00000341838.5:p.Ala116= | |
ENST00000585806.5:n.347A= | ||
ENST00000586669.5:n.356A= | ||
ENST00000587176.5:n.532A= | ||
ENST00000587871.1:c.967A= | ||
ENST00000588882.1:c.273A= | ENSP00000466729.1:p.Ala91= | |
ENST00000590463.1:n.520A= | ||
NM_000363.4:c.348A= , LRG_432t1:c.348A= | NP_000354.4:p.Ala116= | |
NM_000363.5:c.348A= MANE Select | NP_000354.4:p.Ala116= |