HGVS | Genome Assembly |
---|---|
NC_000020.11:g.35699657G>A , CM000682.2:g.35699657G>A | GRCh38 |
NC_000020.10:g.34287579G>A , CM000682.1:g.34287579G>A | GRCh37 |
NC_000020.9:g.33750993G>A | NCBI36 |
NG_033237.1:g.4709C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374077.8:c.25G>A MANE Select | ENSP00000363190.3:p.Gly9Arg | |
ENST00000336695.4:c.25G>A | ENSP00000338293.4:p.Gly9Arg | |
ENST00000374072.5:c.25G>A | ENSP00000363185.1:p.Gly9Arg | |
ENST00000374077.7:c.25G>A | ENSP00000363190.3:p.Gly9Arg | |
ENST00000374078.5:c.25G>A | ENSP00000363191.1:p.Gly9Arg | |
ENST00000397416.1:c.25G>A | ENSP00000380561.1:p.Gly9Arg | |
NM_080748.2:c.25G>A | NP_542786.1:p.Gly9Arg | |
XM_017027678.1:c.25G>A | XP_016883167.1:p.Gly9Arg | |
NM_080748.3:c.25G>A MANE Select | NP_542786.1:p.Gly9Arg |