HGVS | Genome Assembly |
---|---|
NC_000018.10:g.7015797G= , CM000680.2:g.7015797G= | GRCh38 |
NC_000018.9:g.7015796G= , CM000680.1:g.7015796G= | GRCh37 |
NC_000018.8:g.7005796G= | NCBI36 |
NG_034251.1:g.107018C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389658.4:c.3051C= MANE Select | ENSP00000374309.3:p.Pro1017= | |
ENST00000389658.3:c.3051C= | ENSP00000374309.3:p.Pro1017= | |
ENST00000579014.5:n.4066C= | ||
NM_005559.3:c.3051C= | NP_005550.2:p.Pro1017= | |
XM_011525655.1:c.3051C= | XP_011523957.1:p.Pro1017= | |
XM_011525656.1:c.1479C= | XP_011523958.1:p.Pro493= | |
XM_011525657.1:c.3051C= | XP_011523959.1:p.Pro1017= | |
XM_011525655.2:c.3051C= | XP_011523957.1:p.Pro1017= | |
XM_011525656.2:c.1479C= | XP_011523958.1:p.Pro493= | |
NM_005559.4:c.3051C= MANE Select | NP_005550.2:p.Pro1017= |