HGVS | Genome Assembly |
---|---|
NC_000019.10:g.41970282C>T , CM000681.2:g.41970282C>T | GRCh38 |
NC_000019.9:g.42474434C>T , CM000681.1:g.42474434C>T | GRCh37 |
NC_000019.8:g.47166274C>T | NCBI36 |
NG_008015.1:g.28949G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545399.6:c.2484G>A | ENSP00000444688.1:p.Glu828= | |
ENST00000644613.1:c.2445G>A | ENSP00000494711.1:p.Glu815= | |
ENST00000648268.1:c.2445G>A MANE Select | ENSP00000498113.1:p.Glu815= | |
ENST00000302102.9:c.2445G>A | ENSP00000302397.5:p.Glu815= | |
ENST00000441343.5:c.2445G>A | ENSP00000411503.1:p.Glu815= | |
ENST00000543770.5:c.2478G>A | ENSP00000437577.1:p.Glu826= | |
ENST00000545399.5:c.2484G>A | ENSP00000444688.1:p.Glu828= | |
ENST00000602133.5:c.2355G>A | ENSP00000471581.1:p.Glu785= | |
NM_001256213.1:c.2478G>A | NP_001243142.1:p.Glu826= | |
NM_001256214.1:c.2484G>A | NP_001243143.1:p.Glu828= | |
NM_152296.4:c.2445G>A | NP_689509.1:p.Glu815= | |
XM_011526991.1:c.2355G>A | XP_011525293.1:p.Glu785= | |
NM_152296.5:c.2445G>A MANE Select | NP_689509.1:p.Glu815= | |
NM_001256214.2:c.2484G>A | NP_001243143.1:p.Glu828= | |
NM_001256213.2:c.2478G>A | NP_001243142.1:p.Glu826= |