HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161219158_161219159del , CM000663.2:g.161219158_161219159del | GRCh38 |
NC_000001.10:g.161188948_161188949del , CM000663.1:g.161188948_161188949del | GRCh37 |
NC_000001.9:g.159455572_159455573del | NCBI36 |
NG_029043.1:g.8862_8863del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289902.2:c.*215_*216del MANE Select | ENSP00000289902.1:n.*215_*216del | |
ENST00000289902.1:c.*215_*216del | ENSP00000289902.1:n.*215_*216del | |
ENST00000367992.7:c.198+435_198+436del | ENSP00000356971.3:n.198+435_198+436del | |
ENST00000490414.1:n.472_473del | ||
NM_004106.1:c.*215_*216del | NP_004097.1:n.*215_*216del | |
NM_004106.2:c.*215_*216del MANE Select | NP_004097.1:n.*215_*216del |