HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154092C>A , CM000681.2:g.55154092C>A | GRCh38 |
NC_000019.9:g.55665460C>A , CM000681.1:g.55665460C>A | GRCh37 |
NC_000019.8:g.60357272C>A | NCBI36 |
NG_007866.2:g.8641G>T , LRG_432:g.8641G>T | |
NG_011829.2:g.147G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.487G>T MANE Select | ENSP00000341838.5:p.Ala163Ser | |
ENST00000665070.1:c.520G>T | ENSP00000499482.1:p.Ala174Ser | |
ENST00000344887.9:c.487G>T | ENSP00000341838.5:p.Ala163Ser | |
ENST00000585806.5:n.486G>T | ||
ENST00000588882.1:c.412G>T | ENSP00000466729.1:p.Ala138Ser | |
ENST00000589864.1:n.315G>T | ||
NM_000363.4:c.487G>T , LRG_432t1:c.487G>T | NP_000354.4:p.Ala163Ser | |
NM_000363.5:c.487G>T MANE Select | NP_000354.4:p.Ala163Ser |