HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063575G>A , CM000663.2:g.55063575G>A | GRCh38 |
NC_000001.10:g.55529248G>A , CM000663.1:g.55529248G>A | GRCh37 |
NC_000001.9:g.55301836G>A | NCBI36 |
NG_009061.1:g.29029G>A , LRG_275:g.29029G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*410G>A | ENSP00000501161.2:n.*410G>A | |
ENST00000710286.1:c.2427G>A | ENSP00000518176.1:p.Glu809= | |
ENST00000673903.1:c.1695G>A | ENSP00000501257.1:p.Glu565= | |
ENST00000302118.5:c.2070G>A MANE Select | ENSP00000303208.5:p.Glu690= | |
ENST00000490692.1:n.2616G>A | ||
NM_174936.3:c.2070G>A , LRG_275t1:c.2070G>A | NP_777596.2:p.Glu690= | |
NR_110451.1:n.1677G>A | ||
XM_011541193.1:c.1191G>A | XP_011539495.1:p.Glu397= | |
NM_174936.4:c.2070G>A MANE Select | NP_777596.2:p.Glu690= | |
NR_110451.2:n.1677G>A |