HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610407_1610413del , CM000668.2:g.1610407_1610413del | GRCh38 |
NC_000006.11:g.1610642_1610648del , CM000668.1:g.1610642_1610648del | GRCh37 |
NC_000006.10:g.1555641_1555647del | NCBI36 |
NG_009368.1:g.4962_4968del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645831.2:c.-39_-33del MANE Select | ENSP00000493906.1:n.-39_-33del | |
ENST00000380874.3:c.-39_-33del | ENSP00000370256.2:n.-39_-33del | |
NM_001453.3:c.-39_-33del MANE Select | NP_001444.2:n.-39_-33del |