HGVS | Genome Assembly |
---|---|
NC_000012.12:g.14977906_14977916del , CM000674.2:g.14977906_14977916del | GRCh38 |
NC_000012.11:g.15130840_15130850del , CM000674.1:g.15130840_15130850del | GRCh37 |
NC_000012.10:g.15022107_15022117del | NCBI36 |
NG_016859.1:g.9885_9895del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266395.3:c.-41-66_-41-56del MANE Select | ENSP00000266395.2:n.-41-66_-41-56del | |
ENST00000266395.2:c.-41-66_-41-56del | ENSP00000266395.2:n.-41-66_-41-56del | |
NM_006205.2:c.-41-66_-41-56del | NP_006196.1:n.-41-66_-41-56del | |
XR_931376.1:n.175+11576_175+11586del | ||
XM_017019431.2:c.-107_-97del | XP_016874920.1:n.-107_-97del | |
XR_931376.2:n.389+11576_389+11586del | ||
NM_006205.3:c.-41-66_-41-56del MANE Select | NP_006196.1:n.-41-66_-41-56del |