HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154097G>T , CM000681.2:g.55154097G>T | GRCh38 |
NC_000019.9:g.55665465G>T , CM000681.1:g.55665465G>T | GRCh37 |
NC_000019.8:g.60357277G>T | NCBI36 |
NG_007866.2:g.8636C>A , LRG_432:g.8636C>A | |
NG_011829.2:g.142C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.482C>A MANE Select | ENSP00000341838.5:p.Ala161Asp | |
ENST00000665070.1:c.515C>A | ENSP00000499482.1:p.Ala172Asp | |
ENST00000344887.9:c.482C>A | ENSP00000341838.5:p.Ala161Asp | |
ENST00000585806.5:n.481C>A | ||
ENST00000588882.1:c.407C>A | ENSP00000466729.1:p.Ala136Asp | |
ENST00000589864.1:n.310C>A | ||
NM_000363.4:c.482C>A , LRG_432t1:c.482C>A | NP_000354.4:p.Ala161Asp | |
NM_000363.5:c.482C>A MANE Select | NP_000354.4:p.Ala161Asp |