HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169552295G= , CM000663.2:g.169552295G= | GRCh38 |
NC_000001.10:g.169521533G= , CM000663.1:g.169521533G= | GRCh37 |
NC_000001.9:g.167788157G= | NCBI36 |
NG_011806.1:g.39237C= , LRG_553:g.39237C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.1296+262C= MANE Select | ENSP00000356771.3:n.1296+262C= | |
ENST00000367796.3:c.1296+262C= | ENSP00000356770.3:n.1296+262C= | |
ENST00000367797.7:c.1296+262C= | ENSP00000356771.3:n.1296+262C= | |
NM_000130.4:c.1296+262C= , LRG_553t1:c.1296+262C= | NP_000121.2:n.1296+262C= | |
XM_017000660.2:c.885+262C= | XP_016856149.1:n.885+262C= | |
NM_000130.5:c.1296+262C= MANE Select | NP_000121.2:n.1296+262C= |