HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443586C= , CM000668.2:g.32443586C= | GRCh38 |
NC_000006.11:g.32411363C= , CM000668.1:g.32411363C= | GRCh37 |
NC_000006.10:g.32519341C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.610+120C= MANE Select | ENSP00000378786.2:n.610+120C= | |
ENST00000374982.5:c.535+120C= | ENSP00000364121.5:n.535+120C= | |
ENST00000395388.6:c.610+120C= | ENSP00000378786.2:n.610+120C= | |
NM_019111.4:c.610+120C= | NP_061984.2:n.610+120C= | |
NM_019111.5:c.610+120C= MANE Select | NP_061984.2:n.610+120C= |