HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990531_45990532insGGCG , CM000683.2:g.45990531_45990532insGGCG | GRCh38 |
NC_000021.8:g.47410445_47410446insGGCG , CM000683.1:g.47410445_47410446insGGCG | GRCh37 |
NC_000021.7:g.46234873_46234874insGGCG | NCBI36 |
NG_008674.1:g.13783_13784insGGCG , LRG_475:g.13783_13784insGGCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+109_1002+110insGGCG MANE Select | ENSP00000355180.3:n.1002+109_1002+110insGGCG | |
ENST00000361866.7:c.1002+109_1002+110insGGCG | ENSP00000355180.3:n.1002+109_1002+110insGGCG | |
ENST00000612273.1:c.1002+109_1002+110insGGCG | ENSP00000483630.1:n.1002+109_1002+110insGGCG | |
NM_001848.2:c.1002+109_1002+110insGGCG , LRG_475t1:c.1002+109_1002+110insGGCG | NP_001839.2:n.1002+109_1002+110insGGCG | |
NM_001848.3:c.1002+109_1002+110insGGCG MANE Select | NP_001839.2:n.1002+109_1002+110insGGCG |