HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665409_39665410delinsGC , CM000679.2:g.39665409_39665410delinsGC | GRCh38 |
NC_000017.10:g.37821662_37821663delinsGC , CM000679.1:g.37821662_37821663delinsGC | GRCh37 |
NC_000017.9:g.35075188_35075189delinsGC | NCBI36 |
NG_008892.1:g.5064_5065delinsGC , LRG_210:g.5064_5065delinsGC | |
NG_042278.1:g.2429_2430delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.50_51delinsGC MANE Select | ENSP00000312624.2:p.Arg17= | |
ENST00000309889.2:c.50_51delinsGC | ENSP00000312624.2:p.Arg17= | |
ENST00000578283.1:c.50_51delinsGC | ENSP00000462787.1:p.Arg17= | |
NM_003673.3:c.50_51delinsGC , LRG_210t1:c.50_51delinsGC | NP_003664.1:p.Arg17= | |
NM_003673.4:c.50_51delinsGC MANE Select | NP_003664.1:p.Arg17= |