HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94062517_94062518insCC , CM000663.2:g.94062517_94062518insCC | GRCh38 |
NC_000001.10:g.94528073_94528074insCC , CM000663.1:g.94528073_94528074insCC | GRCh37 |
NC_000001.9:g.94300661_94300662insCC | NCBI36 |
NG_009073.1:g.63632_63633insGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.1937+59_1937+60insGG MANE Select | ENSP00000359245.3:n.1937+59_1937+60insGG | |
ENST00000649773.1:c.1937+59_1937+60insGG | ENSP00000496882.1:n.1937+59_1937+60insGG | |
ENST00000370225.3:c.1937+59_1937+60insGG | ENSP00000359245.3:n.1937+59_1937+60insGG | |
ENST00000536513.5:c.-65+656_-65+657insGG | ENSP00000439707.2:n.-65+656_-65+657insGG | |
NM_000350.2:c.1937+59_1937+60insGG | NP_000341.2:n.1937+59_1937+60insGG | |
NM_000350.3:c.1937+59_1937+60insGG MANE Select | NP_000341.2:n.1937+59_1937+60insGG |