HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21196780_21196781insAAAG , CM000674.2:g.21196780_21196781insAAAG | GRCh38 |
NC_000012.11:g.21349714_21349715insAAAG , CM000674.1:g.21349714_21349715insAAAG | GRCh37 |
NC_000012.10:g.21240981_21240982insAAAG | NCBI36 |
NG_011745.1:g.70587_70588insAAAG , LRG_1022:g.70587_70588insAAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.728-166_728-165insAAAG MANE Select | ENSP00000256958.2:n.728-166_728-165insAAAG | |
ENST00000256958.2:c.728-166_728-165insAAAG | ENSP00000256958.2:n.728-166_728-165insAAAG | |
NM_006446.4:c.728-166_728-165insAAAG , LRG_1022t1:c.728-166_728-165insAAAG | NP_006437.3:n.728-166_728-165insAAAG | |
NM_006446.5:c.728-166_728-165insAAAG MANE Select | NP_006437.3:n.728-166_728-165insAAAG |