HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129531078_129531084del , CM000665.2:g.129531078_129531084del | GRCh38 |
NC_000003.11:g.129249921_129249927del , CM000665.1:g.129249921_129249927del | GRCh37 |
NC_000003.10:g.130732611_130732617del | NCBI36 |
NG_009115.1:g.7440_7446del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.530+34_530+40del MANE Select | ENSP00000296271.3:n.530+34_530+40del | |
ENST00000296271.3:c.530+34_530+40del | ENSP00000296271.3:n.530+34_530+40del | |
NM_000539.3:c.530+34_530+40del MANE Select | NP_000530.1:n.530+34_530+40del |