HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990526_45990527insA , CM000683.2:g.45990526_45990527insA | GRCh38 |
NC_000021.8:g.47410440_47410441insA , CM000683.1:g.47410440_47410441insA | GRCh37 |
NC_000021.7:g.46234868_46234869insA | NCBI36 |
NG_008674.1:g.13778_13779insA , LRG_475:g.13778_13779insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+104_1002+105insA MANE Select | ENSP00000355180.3:n.1002+104_1002+105insA | |
ENST00000361866.7:c.1002+104_1002+105insA | ENSP00000355180.3:n.1002+104_1002+105insA | |
ENST00000612273.1:c.1002+104_1002+105insA | ENSP00000483630.1:n.1002+104_1002+105insA | |
NM_001848.2:c.1002+104_1002+105insA , LRG_475t1:c.1002+104_1002+105insA | NP_001839.2:n.1002+104_1002+105insA | |
NM_001848.3:c.1002+104_1002+105insA MANE Select | NP_001839.2:n.1002+104_1002+105insA |