HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55156195C= , CM000681.2:g.55156195C= | GRCh38 |
NC_000019.9:g.55667563C= , CM000681.1:g.55667563C= | GRCh37 |
NC_000019.8:g.60359375C= | NCBI36 |
NG_007866.2:g.6538G= , LRG_432:g.6538G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.282+6G= MANE Select | ENSP00000341838.5:n.282+6G= | |
ENST00000665070.1:c.282+6G= | ENSP00000499482.1:n.282+6G= | |
ENST00000344887.9:c.282+6G= | ENSP00000341838.5:n.282+6G= | |
ENST00000585806.5:n.281+6G= | ||
ENST00000586669.5:n.290+6G= | ||
ENST00000587176.5:n.466+6G= | ||
ENST00000587871.1:c.901+6G= | ||
ENST00000588882.1:c.207+6G= | ENSP00000466729.1:n.207+6G= | |
ENST00000590463.1:n.454+6G= | ||
NM_000363.4:c.282+6G= , LRG_432t1:c.282+6G= | NP_000354.4:n.282+6G= | |
NM_000363.5:c.282+6G= MANE Select | NP_000354.4:n.282+6G= |