HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152307668_152307669insTCC , CM000663.2:g.152307668_152307669insTCC | GRCh38 |
NC_000001.10:g.152280144_152280145insTCC , CM000663.1:g.152280144_152280145insTCC | GRCh37 |
NC_000001.9:g.150546768_150546769insTCC | NCBI36 |
NG_016190.1:g.22535_22536insGGA , LRG_1028:g.22535_22536insGGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.7217_7218insGGA MANE Select | ENSP00000357789.1:p.Gly2406_Arg2407insGlu | |
ENST00000368799.1:c.7217_7218insGGA | ENSP00000357789.1:p.Gly2406_Arg2407insGlu | |
NM_002016.1:c.7217_7218insGGA , LRG_1028t1:c.7217_7218insGGA | NP_002007.1:p.Gly2406_Arg2407insGlu | |
XM_011509329.1:c.7217_7218insGGA | XP_011507631.1:p.Gly2406_Arg2407insGlu | |
NM_002016.2:c.7217_7218insGGA MANE Select | NP_002007.1:p.Gly2406_Arg2407insGlu |