HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215734_21215737delinsTAAG , CM000674.2:g.21215734_21215737delinsTAAG | GRCh38 |
NC_000012.11:g.21368668_21368671delinsTAAG , CM000674.1:g.21368668_21368671delinsTAAG | GRCh37 |
NC_000012.10:g.21259935_21259938delinsTAAG | NCBI36 |
NG_011745.1:g.89541_89544delinsTAAG , LRG_1022:g.89541_89544delinsTAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1385_1498-1382delinsTAAG MANE Select | ENSP00000256958.2:n.1498-1385_1498-1382de... | |
ENST00000256958.2:c.1498-1385_1498-1382delinsTAAG | ENSP00000256958.2:n.1498-1385_1498-1382de... | |
NM_006446.4:c.1498-1385_1498-1382delinsTAAG , LRG_1022t1:c.1498-1385_1498-1382delinsTAAG | NP_006437.3:n.1498-1385_1498-1382delinsTA... | |
NM_006446.5:c.1498-1385_1498-1382delinsTAAG MANE Select | NP_006437.3:n.1498-1385_1498-1382delinsTA... |