HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176732_21176735del , CM000674.2:g.21176732_21176735del | GRCh38 |
NC_000012.11:g.21329666_21329669del , CM000674.1:g.21329666_21329669del | GRCh37 |
NC_000012.10:g.21220933_21220936del | NCBI36 |
NG_011745.1:g.50539_50542del , LRG_1022:g.50539_50542del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.360-44_360-41del MANE Select | ENSP00000256958.2:n.360-44_360-41del | |
ENST00000256958.2:c.360-44_360-41del | ENSP00000256958.2:n.360-44_360-41del | |
ENST00000543498.5:c.426-44_426-41del | ||
NM_006446.4:c.360-44_360-41del , LRG_1022t1:c.360-44_360-41del | NP_006437.3:n.360-44_360-41del | |
NM_006446.5:c.360-44_360-41del MANE Select | NP_006437.3:n.360-44_360-41del |