HGVS | Genome Assembly |
---|---|
NC_000018.10:g.7015738G= , CM000680.2:g.7015738G= | GRCh38 |
NC_000018.9:g.7015737G= , CM000680.1:g.7015737G= | GRCh37 |
NC_000018.8:g.7005737G= | NCBI36 |
NG_034251.1:g.107077C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000389658.4:c.3110C= MANE Select | ENSP00000374309.3:p.Ala1037= | |
ENST00000389658.3:c.3110C= | ENSP00000374309.3:p.Ala1037= | |
ENST00000579014.5:n.4125C= | ||
NM_005559.3:c.3110C= | NP_005550.2:p.Ala1037= | |
XM_011525655.1:c.3110C= | XP_011523957.1:p.Ala1037= | |
XM_011525656.1:c.1538C= | XP_011523958.1:p.Ala513= | |
XM_011525657.1:c.3110C= | XP_011523959.1:p.Ala1037= | |
XM_011525655.2:c.3110C= | XP_011523957.1:p.Ala1037= | |
XM_011525656.2:c.1538C= | XP_011523958.1:p.Ala513= | |
NM_005559.4:c.3110C= MANE Select | NP_005550.2:p.Ala1037= |