HGVS | Genome Assembly |
---|---|
NC_000004.12:g.119320670_119320672delinsCCT , CM000666.2:g.119320670_119320672delinsCCT | GRCh38 |
NC_000004.11:g.120241825_120241827delinsCCT , CM000666.1:g.120241825_120241827delinsCCT | GRCh37 |
NC_000004.10:g.120461273_120461275delinsCCT | NCBI36 |
NG_011444.1:g.6490_6492delinsAGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000274024.4:c.238_240delinsAGG MANE Select | ENSP00000274024.3:p.Arg80= | |
ENST00000274024.3:c.238_240delinsAGG | ENSP00000274024.3:p.Arg80= | |
NM_000134.3:c.238_240delinsAGG | NP_000125.2:p.Arg80= | |
NM_000134.4:c.238_240delinsAGG MANE Select | NP_000125.2:p.Arg80= |