HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063584A>T , CM000663.2:g.55063584A>T | GRCh38 |
NC_000001.10:g.55529257A>T , CM000663.1:g.55529257A>T | GRCh37 |
NC_000001.9:g.55301845A>T | NCBI36 |
NG_009061.1:g.29038A>T , LRG_275:g.29038A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*419A>T | ENSP00000501161.2:n.*419A>T | |
ENST00000710286.1:c.2436A>T | ENSP00000518176.1:p.Ter812Cys | |
ENST00000673903.1:c.1704A>T | ENSP00000501257.1:p.Ter568Cys | |
ENST00000302118.5:c.2079A>T MANE Select | ENSP00000303208.5:p.Ter693Cys | |
ENST00000490692.1:n.2625A>T | ||
NM_174936.3:c.2079A>T , LRG_275t1:c.2079A>T | NP_777596.2:p.Ter693Cys | |
NR_110451.1:n.1686A>T | ||
XM_011541193.1:c.1200A>T | XP_011539495.1:p.Ter400Cys | |
NM_174936.4:c.2079A>T MANE Select | NP_777596.2:p.Ter693Cys | |
NR_110451.2:n.1686A>T |