HGVS | Genome Assembly |
---|---|
NC_000012.12:g.14977953_14977954dup , CM000674.2:g.14977953_14977954dup | GRCh38 |
NC_000012.11:g.15130887_15130888dup , CM000674.1:g.15130887_15130888dup | GRCh37 |
NC_000012.10:g.15022154_15022155dup | NCBI36 |
NG_016859.1:g.9932_9933dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266395.3:c.-41-19_-41-18dup MANE Select | ENSP00000266395.2:n.-41-19_-41-18dup | |
ENST00000266395.2:c.-41-19_-41-18dup | ENSP00000266395.2:n.-41-19_-41-18dup | |
NM_006205.2:c.-41-19_-41-18dup | NP_006196.1:n.-41-19_-41-18dup | |
XR_931376.1:n.175+11539_175+11540dup | ||
XM_017019431.2:c.-60_-59dup | XP_016874920.1:n.-60_-59dup | |
XR_931376.2:n.389+11539_389+11540dup | ||
NM_006205.3:c.-41-19_-41-18dup MANE Select | NP_006196.1:n.-41-19_-41-18dup |