HGVS | Genome Assembly |
---|---|
NC_000003.12:g.184060004_184060005delinsAA , CM000665.2:g.184060004_184060005delinsAA | GRCh38 |
NC_000003.11:g.183777792_183777793delinsAA , CM000665.1:g.183777792_183777793delinsAA | GRCh37 |
NC_000003.10:g.185260486_185260487delinsAA | NCBI36 |
NG_012749.1:g.11958_11959delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000318351.2:c.1102_1103delinsAA MANE Select | ENSP00000322617.1:p.Gly368Lys | |
ENST00000318351.1:c.1102_1103delinsAA | ENSP00000322617.1:p.Gly368Lys | |
NM_130770.2:c.1102_1103delinsAA | NP_570126.2:p.Gly368Lys | |
NM_130770.3:c.1102_1103delinsAA MANE Select | NP_570126.2:p.Gly368Lys |