HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81646522_81646524del , CM000665.2:g.81646522_81646524del | GRCh38 |
NC_000003.11:g.81695673_81695675del , CM000665.1:g.81695673_81695675del | GRCh37 |
NC_000003.10:g.81778363_81778365del | NCBI36 |
NG_011810.1:g.120277_120279del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.692-42_692-40del MANE Select | ENSP00000410833.2:n.692-42_692-40del | |
ENST00000429644.6:c.692-42_692-40del | ENSP00000410833.2:n.692-42_692-40del | |
ENST00000489715.1:c.569-42_569-40del | ENSP00000419638.1:n.569-42_569-40del | |
ENST00000498468.1:n.220-20_220-18del | ||
NM_000158.3:c.692-42_692-40del | NP_000149.3:n.692-42_692-40del | |
NM_000158.4:c.692-42_692-40del MANE Select | NP_000149.4:n.692-42_692-40del |