HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32441002_32441003del , CM000668.2:g.32441002_32441003del | GRCh38 |
NC_000006.11:g.32408779_32408780del , CM000668.1:g.32408779_32408780del | GRCh37 |
NC_000006.10:g.32516757_32516758del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.82+970_82+971del MANE Select | ENSP00000378786.2:n.82+970_82+971del | |
ENST00000374982.5:c.82+970_82+971del | ENSP00000364121.5:n.82+970_82+971del | |
ENST00000395388.6:c.82+970_82+971del | ENSP00000378786.2:n.82+970_82+971del | |
NM_019111.4:c.82+970_82+971del | NP_061984.2:n.82+970_82+971del | |
NM_019111.5:c.82+970_82+971del MANE Select | NP_061984.2:n.82+970_82+971del |