HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21196932_21196935del , CM000674.2:g.21196932_21196935del | GRCh38 |
NC_000012.11:g.21349866_21349869del , CM000674.1:g.21349866_21349869del | GRCh37 |
NC_000012.10:g.21241133_21241136del | NCBI36 |
NG_011745.1:g.70739_70742del , LRG_1022:g.70739_70742del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.728-14_728-11del MANE Select | ENSP00000256958.2:n.728-14_728-11del | |
ENST00000256958.2:c.728-14_728-11del | ENSP00000256958.2:n.728-14_728-11del | |
NM_006446.4:c.728-14_728-11del , LRG_1022t1:c.728-14_728-11del | NP_006437.3:n.728-14_728-11del | |
NM_006446.5:c.728-14_728-11del MANE Select | NP_006437.3:n.728-14_728-11del |