HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461638_122461643del , CM000672.2:g.122461638_122461643del | GRCh38 |
NC_000010.10:g.124221154_124221159del , CM000672.1:g.124221154_124221159del | GRCh37 |
NC_000010.9:g.124211144_124211149del | NCBI36 |
NG_011554.1:g.5114_5119del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-15_-10del MANE Select | ENSP00000357980.3:n.-15_-10del | |
ENST00000648167.1:c.154+2929_154+2934del | ENSP00000498033.1:n.154+2929_154+2934del | |
ENST00000368984.7:c.-15_-10del | ENSP00000357980.3:n.-15_-10del | |
NM_002775.4:c.-15_-10del | NP_002766.1:n.-15_-10del | |
NM_002775.5:c.-15_-10del MANE Select | NP_002766.1:n.-15_-10del |