HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94062522_94062531del , CM000663.2:g.94062522_94062531del | GRCh38 |
NC_000001.10:g.94528078_94528087del , CM000663.1:g.94528078_94528087del | GRCh37 |
NC_000001.9:g.94300666_94300675del | NCBI36 |
NG_009073.1:g.63620_63629del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.1937+47_1937+56del MANE Select | ENSP00000359245.3:n.1937+47_1937+56del | |
ENST00000649773.1:c.1937+47_1937+56del | ENSP00000496882.1:n.1937+47_1937+56del | |
ENST00000370225.3:c.1937+47_1937+56del | ENSP00000359245.3:n.1937+47_1937+56del | |
ENST00000536513.5:c.-65+644_-65+653del | ENSP00000439707.2:n.-65+644_-65+653del | |
NM_000350.2:c.1937+47_1937+56del | NP_000341.2:n.1937+47_1937+56del | |
NM_000350.3:c.1937+47_1937+56del MANE Select | NP_000341.2:n.1937+47_1937+56del |