HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957932_19957933delinsGA , CM000670.2:g.19957932_19957933delinsGA | GRCh38 |
NC_000008.10:g.19815443_19815444delinsGA , CM000670.1:g.19815443_19815444delinsGA | GRCh37 |
NC_000008.9:g.19859723_19859724delinsGA | NCBI36 |
NG_008855.1:g.23862_23863delinsGA | |
NG_008855.2:g.61216_61217delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.1019-1328_1019-1327delinsGA MANE Select | ENSP00000497642.1:n.1019-1328_1019-1327delinsGA | |
ENST00000650478.1:c.79+1849_79+1850delinsGA | ENSP00000497560.1:n.79+1849_79+1850delinsGA | |
ENST00000311322.8:c.1019-1328_1019-1327delinsGA | ENSP00000309757.6:n.1019-1328_1019-1327delinsGA | |
NM_000237.2:c.1019-1328_1019-1327delinsGA | NP_000228.1:n.1019-1328_1019-1327delinsGA | |
NM_000237.3:c.1019-1328_1019-1327delinsGA MANE Select | NP_000228.1:n.1019-1328_1019-1327delinsGA |