HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154780T>A , CM000681.2:g.55154780T>A | GRCh38 |
NC_000019.9:g.55666148T>A , CM000681.1:g.55666148T>A | GRCh37 |
NC_000019.8:g.60357960T>A | NCBI36 |
NG_007866.2:g.7953A>T , LRG_432:g.7953A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.333A>T MANE Select | ENSP00000341838.5:p.Arg111Ser | |
ENST00000665070.1:c.333A>T | ENSP00000499482.1:p.Arg111Ser | |
ENST00000344887.9:c.333A>T | ENSP00000341838.5:p.Arg111Ser | |
ENST00000585806.5:n.332A>T | ||
ENST00000586669.5:n.341A>T | ||
ENST00000587176.5:n.517A>T | ||
ENST00000587871.1:c.952A>T | ||
ENST00000588882.1:c.258A>T | ENSP00000466729.1:p.Arg86Ser | |
ENST00000590463.1:n.505A>T | ||
NM_000363.4:c.333A>T , LRG_432t1:c.333A>T | NP_000354.4:p.Arg111Ser | |
NM_000363.5:c.333A>T MANE Select | NP_000354.4:p.Arg111Ser |