HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269515T= , CM000668.2:g.31269515T= | GRCh38 |
NC_000006.11:g.31237292T= , CM000668.1:g.31237292T= | GRCh37 |
NC_000006.10:g.31345271T= | NCBI36 |
NG_029422.2:g.7617A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.1026A= MANE Select | ENSP00000365402.5:p.Gly342= | |
ENST00000376228.9:c.1026A= | ENSP00000365402.5:p.Gly342= | |
ENST00000376237.8:c.*613A= | ENSP00000365412.4:n.*613A= | |
ENST00000383329.7:c.1044A= | ENSP00000372819.3:p.Gly348= | |
ENST00000466892.5:n.152A= | ||
ENST00000470363.5:n.784A= | ||
ENST00000487245.5:n.1385A= | ||
NM_002117.5:c.1026A= | NP_002108.4:p.Gly342= | |
NM_002117.6:c.1026A= MANE Select | NP_002108.4:p.Gly342= |