HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188991588_188991606del , CM000664.2:g.188991588_188991606del | GRCh38 |
NC_000002.11:g.189856314_189856332del , CM000664.1:g.189856314_189856332del | GRCh37 |
NC_000002.10:g.189564559_189564577del | NCBI36 |
NG_007404.1:g.22216_22234del , LRG_3:g.22216_22234del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.897+57_898-63del | ENSP00000415346.2:n.897+57_898-63del | |
ENST00000304636.9:c.897+57_898-63del MANE Select | ENSP00000304408.4:n.897+57_898-63del | |
ENST00000304636.7:c.897+57_898-63del | ENSP00000304408.3:n.897+57_898-63del | |
ENST00000317840.9:c.897+57_898-63del | ENSP00000315243.6:n.897+57_898-63del | |
NM_000090.3:c.897+57_898-63del , LRG_3t1:c.897+57_898-63del | NP_000081.1:n.897+57_898-63del | |
NM_000090.4:c.897+57_898-63del MANE Select | NP_000081.2:n.897+57_898-63del |