HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71994620_71994621delinsAG , CM000674.2:g.71994620_71994621delinsAG | GRCh38 |
NC_000012.11:g.72388400_72388401delinsAG , CM000674.1:g.72388400_72388401delinsAG | GRCh37 |
NC_000012.10:g.70674667_70674668delinsAG | NCBI36 |
NG_008279.1:g.60775_60776delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333850.4:c.1068+55_1068+56delinsAG MANE Select | ENSP00000329093.3:n.1068+55_1068+56delins... | |
ENST00000333850.3:c.1068+55_1068+56delinsAG | ENSP00000329093.3:n.1068+55_1068+56delins... | |
NM_173353.3:c.1068+55_1068+56delinsAG | NP_775489.2:n.1068+55_1068+56delinsAG | |
XM_011537899.1:c.474+55_474+56delinsAG | XP_011536201.1:n.474+55_474+56delinsAG | |
NM_173353.4:c.1068+55_1068+56delinsAG MANE Select | NP_775489.2:n.1068+55_1068+56delinsAG |