HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81646389del , CM000665.2:g.81646389del | GRCh38 |
NC_000003.11:g.81695540del , CM000665.1:g.81695540del | GRCh37 |
NC_000003.10:g.81778230del | NCBI36 |
NG_011810.1:g.120415del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.782+6del MANE Select | ENSP00000410833.2:n.782+6del | |
ENST00000429644.6:c.782+6del | ENSP00000410833.2:n.782+6del | |
ENST00000489715.1:c.659+6del | ENSP00000419638.1:n.659+6del | |
ENST00000498468.1:n.332+6del | ||
NM_000158.3:c.782+6del | NP_000149.3:n.782+6del | |
NM_000158.4:c.782+6del MANE Select | NP_000149.4:n.782+6del |