HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21178454_21178455delinsAT , CM000674.2:g.21178454_21178455delinsAT | GRCh38 |
NC_000012.11:g.21331388_21331389delinsAT , CM000674.1:g.21331388_21331389delinsAT | GRCh37 |
NC_000012.10:g.21222655_21222656delinsAT | NCBI36 |
NG_011745.1:g.52261_52262delinsAT , LRG_1022:g.52261_52262delinsAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.482-122_482-121delinsAT MANE Select | ENSP00000256958.2:n.482-122_482-121delinsAT | |
ENST00000256958.2:c.482-122_482-121delinsAT | ENSP00000256958.2:n.482-122_482-121delinsAT | |
NM_006446.4:c.482-122_482-121delinsAT , LRG_1022t1:c.482-122_482-121delinsAT | NP_006437.3:n.482-122_482-121delinsAT | |
NM_006446.5:c.482-122_482-121delinsAT MANE Select | NP_006437.3:n.482-122_482-121delinsAT |