HGVS | Genome Assembly |
---|---|
NC_000012.12:g.14977954_14977964del , CM000674.2:g.14977954_14977964del | GRCh38 |
NC_000012.11:g.15130888_15130898del , CM000674.1:g.15130888_15130898del | GRCh37 |
NC_000012.10:g.15022155_15022165del | NCBI36 |
NG_016859.1:g.9933_9943del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266395.3:c.-41-18_-41-8del MANE Select | ENSP00000266395.2:n.-41-18_-41-8del | |
ENST00000266395.2:c.-41-18_-41-8del | ENSP00000266395.2:n.-41-18_-41-8del | |
NM_006205.2:c.-41-18_-41-8del | NP_006196.1:n.-41-18_-41-8del | |
XR_931376.1:n.175+11524_175+11534del | ||
XM_017019431.2:c.-59_-49del | XP_016874920.1:n.-59_-49del | |
XR_931376.2:n.389+11524_389+11534del | ||
NM_006205.3:c.-41-18_-41-8del MANE Select | NP_006196.1:n.-41-18_-41-8del |