HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443323_32443325del , CM000668.2:g.32443323_32443325del | GRCh38 |
NC_000006.11:g.32411100_32411102del , CM000668.1:g.32411100_32411102del | GRCh37 |
NC_000006.10:g.32519078_32519080del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.467_469del MANE Select | ENSP00000378786.2:p.Gly156del | |
ENST00000374982.5:c.392_394del | ENSP00000364121.5:p.Gly131del | |
ENST00000395388.6:c.467_469del | ENSP00000378786.2:p.Gly156del | |
NM_019111.4:c.467_469del | NP_061984.2:p.Gly156del | |
NM_019111.5:c.467_469del MANE Select | NP_061984.2:p.Gly156del |