HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24302123_24302124insC , CM000668.2:g.24302123_24302124insC | GRCh38 |
NC_000006.11:g.24302351_24302352insC , CM000668.1:g.24302351_24302352insC | GRCh37 |
NC_000006.10:g.24410330_24410331insC | NCBI36 |
NG_012829.1:g.60929_60930insG | |
NG_012829.2:g.86169_86170insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.349-80_349-79insG MANE Select | ENSP00000367715.3:n.349-80_349-79insG | |
ENST00000378454.7:c.349-80_349-79insG | ENSP00000367715.3:n.349-80_349-79insG | |
NM_001195610.1:c.349-80_349-79insG | NP_001182539.1:n.349-80_349-79insG | |
NM_016356.4:c.349-80_349-79insG | NP_057440.2:n.349-80_349-79insG | |
NM_016356.5:c.349-80_349-79insG MANE Select | NP_057440.2:n.349-80_349-79insG | |
NM_001195610.2:c.349-80_349-79insG | NP_001182539.1:n.349-80_349-79insG |