HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461618del , CM000672.2:g.122461618del | GRCh38 |
NC_000010.10:g.124221134del , CM000672.1:g.124221134del | GRCh37 |
NC_000010.9:g.124211124del | NCBI36 |
NG_011554.1:g.5094del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-35del MANE Select | ENSP00000357980.3:n.-35del | |
ENST00000648167.1:c.154+2909del | ENSP00000498033.1:n.154+2909del | |
ENST00000368984.7:c.-35del | ENSP00000357980.3:n.-35del | |
NM_002775.4:c.-35del | NP_002766.1:n.-35del | |
NM_002775.5:c.-35del MANE Select | NP_002766.1:n.-35del |