HGVS | Genome Assembly |
---|---|
NC_000018.10:g.7015734C= , CM000680.2:g.7015734C= | GRCh38 |
NC_000018.9:g.7015733C= , CM000680.1:g.7015733C= | GRCh37 |
NC_000018.8:g.7005733C= | NCBI36 |
NG_034251.1:g.107081G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389658.4:c.3114G= MANE Select | ENSP00000374309.3:p.Glu1038= | |
ENST00000389658.3:c.3114G= | ENSP00000374309.3:p.Glu1038= | |
ENST00000579014.5:n.4129G= | ||
NM_005559.3:c.3114G= | NP_005550.2:p.Glu1038= | |
XM_011525655.1:c.3114G= | XP_011523957.1:p.Glu1038= | |
XM_011525656.1:c.1542G= | XP_011523958.1:p.Glu514= | |
XM_011525657.1:c.3114G= | XP_011523959.1:p.Glu1038= | |
XM_011525655.2:c.3114G= | XP_011523957.1:p.Glu1038= | |
XM_011525656.2:c.1542G= | XP_011523958.1:p.Glu514= | |
NM_005559.4:c.3114G= MANE Select | NP_005550.2:p.Glu1038= |