HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215636_21215637delinsAG , CM000674.2:g.21215636_21215637delinsAG | GRCh38 |
NC_000012.11:g.21368570_21368571delinsAG , CM000674.1:g.21368570_21368571delinsAG | GRCh37 |
NC_000012.10:g.21259837_21259838delinsAG | NCBI36 |
NG_011745.1:g.89443_89444delinsAG , LRG_1022:g.89443_89444delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1483_1498-1482delinsAG MANE Select | ENSP00000256958.2:n.1498-1483_1498-1482de... | |
ENST00000256958.2:c.1498-1483_1498-1482delinsAG | ENSP00000256958.2:n.1498-1483_1498-1482de... | |
NM_006446.4:c.1498-1483_1498-1482delinsAG , LRG_1022t1:c.1498-1483_1498-1482delinsAG | NP_006437.3:n.1498-1483_1498-1482delinsAG... | |
NM_006446.5:c.1498-1483_1498-1482delinsAG MANE Select | NP_006437.3:n.1498-1483_1498-1482delinsAG... |