HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119413933G>T , CM000665.2:g.119413933G>T | GRCh38 |
NC_000003.11:g.119132780G>T , CM000665.1:g.119132780G>T | GRCh37 |
NC_000003.10:g.120615470G>T | NCBI36 |
NG_007665.2:g.124561G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.2004G>T MANE Select | ENSP00000264245.4:p.Glu668Asp | |
ENST00000264245.8:c.2004G>T | ENSP00000264245.4:p.Glu668Asp | |
NM_020754.3:c.2004G>T | NP_065805.2:p.Glu668Asp | |
XM_005247671.3:c.1911G>T | XP_005247728.1:p.Glu637Asp | |
XM_006713714.2:c.1944G>T | XP_006713777.1:p.Glu648Asp | |
XM_006713714.3:c.1944G>T | XP_006713777.1:p.Glu648Asp | |
XM_017006955.1:c.1512G>T | XP_016862444.1:p.Glu504Asp | |
NM_020754.4:c.2004G>T MANE Select | NP_065805.2:p.Glu668Asp |