HGVS | Genome Assembly |
---|---|
NC_000023.11:g.119929907del , CM000685.2:g.119929907del | GRCh38 |
NC_000023.10:g.119063870del , CM000685.1:g.119063870del | GRCh37 |
NC_000023.9:g.118947898del | NCBI36 |
NG_021260.1:g.18866del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371410.5:c.1073+109del MANE Select | ENSP00000360464.3:n.1073+109del | |
ENST00000652253.1:c.1069+109del | ||
ENST00000371410.4:c.1073+109del | ENSP00000360464.3:n.1073+109del | |
ENST00000477789.5:n.2001+109del | ||
NM_024528.3:c.1073+109del | NP_078804.2:n.1073+109del | |
XM_017029842.1:c.776+109del | XP_016885331.1:n.776+109del | |
NM_024528.4:c.1073+109del MANE Select | NP_078804.2:n.1073+109del |