HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269576T= , CM000668.2:g.31269576T= | GRCh38 |
NC_000006.11:g.31237353T= , CM000668.1:g.31237353T= | GRCh37 |
NC_000006.10:g.31345332T= | NCBI36 |
NG_029422.2:g.7556A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.1016-51A= MANE Select | ENSP00000365402.5:n.1016-51A= | |
ENST00000376228.9:c.1016-51A= | ENSP00000365402.5:n.1016-51A= | |
ENST00000376237.8:c.*603-51A= | ENSP00000365412.4:n.*603-51A= | |
ENST00000383329.7:c.1016-33A= | ENSP00000372819.3:n.1016-33A= | |
ENST00000466892.5:n.91A= | ||
ENST00000470363.5:n.723A= | ||
ENST00000487245.5:n.1375-51A= | ||
NM_002117.5:c.1016-51A= | NP_002108.4:n.1016-51A= | |
NM_002117.6:c.1016-51A= MANE Select | NP_002108.4:n.1016-51A= |