HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65029453C= , CM000677.2:g.65029453C= | GRCh38 |
NC_000015.9:g.65321791C= , CM000677.1:g.65321791C= | GRCh37 |
NC_000015.8:g.63108844C= | NCBI36 |
NG_029184.1:g.5187G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000220058.9:c.161G= MANE Select | ENSP00000220058.4:p.Gly54= | |
ENST00000220058.8:c.161G= | ENSP00000220058.4:p.Gly54= | |
ENST00000543678.1:c.161G= | ENSP00000443754.1:p.Gly54= | |
ENST00000558460.5:c.161G= | ENSP00000452646.1:p.Gly54= | |
ENST00000558614.1:n.122G= | ||
ENST00000559633.1:n.80G= | ||
ENST00000560717.5:c.146G= | ENSP00000457257.1:p.Gly49= | |
NM_139242.3:c.161G= | NP_640335.2:p.Gly54= | |
XM_005254158.5:c.161G= | XP_005254215.2:p.Gly54= | |
XR_001751081.1:n.176G= | ||
NM_139242.4:c.161G= MANE Select | NP_640335.2:p.Gly54= |