HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461595_122461626del , CM000672.2:g.122461595_122461626del | GRCh38 |
NC_000010.10:g.124221111_124221142del , CM000672.1:g.124221111_124221142del | GRCh37 |
NC_000010.9:g.124211101_124211132del | NCBI36 |
NG_011554.1:g.5071_5102del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-58_-27del MANE Select | ENSP00000357980.3:n.-58_-27del | |
ENST00000648167.1:c.154+2886_154+2917del | ENSP00000498033.1:n.154+2886_154+2917del | |
ENST00000368984.7:c.-58_-27del | ENSP00000357980.3:n.-58_-27del | |
NM_002775.4:c.-58_-27del | NP_002766.1:n.-58_-27del | |
NM_002775.5:c.-58_-27del MANE Select | NP_002766.1:n.-58_-27del |