HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443523_32443524del , CM000668.2:g.32443523_32443524del | GRCh38 |
NC_000006.11:g.32411300_32411301del , CM000668.1:g.32411300_32411301del | GRCh37 |
NC_000006.10:g.32519278_32519279del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.610+57_610+58del MANE Select | ENSP00000378786.2:n.610+57_610+58del | |
ENST00000374982.5:c.535+57_535+58del | ENSP00000364121.5:n.535+57_535+58del | |
ENST00000395388.6:c.610+57_610+58del | ENSP00000378786.2:n.610+57_610+58del | |
NM_019111.4:c.610+57_610+58del | NP_061984.2:n.610+57_610+58del | |
NM_019111.5:c.610+57_610+58del MANE Select | NP_061984.2:n.610+57_610+58del |