HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44115645A= , CM000682.2:g.44115645A= | GRCh38 |
NC_000020.10:g.42744285A= , CM000682.1:g.42744285A= | GRCh37 |
NC_000020.9:g.42177699A= | NCBI36 |
NG_031867.1:g.76934T= , LRG_394:g.76934T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.2010+20T= MANE Select | ENSP00000362071.3:n.2010+20T= | |
ENST00000372980.3:c.2010+20T= | ENSP00000362071.3:n.2010+20T= | |
NM_020433.4:c.2010+20T= , LRG_394t1:c.2010+20T= | NP_065166.2:n.2010+20T= | |
XM_006723832.2:c.2010+20T= | XP_006723895.1:n.2010+20T= | |
NM_020433.5:c.2010+20T= MANE Select | NP_065166.2:n.2010+20T= |