HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1612756_1612763del , CM000668.2:g.1612756_1612763del | GRCh38 |
NC_000006.11:g.1612991_1612998del , CM000668.1:g.1612991_1612998del | GRCh37 |
NC_000006.10:g.1557990_1557997del | NCBI36 |
NG_009368.1:g.7311_7318del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.*649_*656del MANE Select | ENSP00000493906.1:n.*649_*656del | |
ENST00000380874.3:c.*649_*656del | ENSP00000370256.2:n.*649_*656del | |
NM_001453.2:c.2311_2318del | NP_001444.2:n.2311_2318del | |
NM_001453.3:c.*649_*656del MANE Select | NP_001444.2:n.*649_*656del |