HGVS | Genome Assembly |
---|---|
NC_000023.11:g.29917558A>T , CM000685.2:g.29917558A>T | GRCh38 |
NC_000023.10:g.29935675A>T , CM000685.1:g.29935675A>T | GRCh37 |
NC_000023.9:g.29845596A>T | NCBI36 |
NG_008292.1:g.1334995A>T | |
NG_008292.2:g.1334995A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378993.6:c.873A>T MANE Select | ENSP00000368278.1:p.Glu291Asp | |
ENST00000302196.5:c.96A>T | ENSP00000305200.5:p.Glu32Asp | |
ENST00000378993.5:c.873A>T | ENSP00000368278.1:p.Glu291Asp | |
NM_014271.3:c.873A>T | NP_055086.1:p.Glu291Asp | |
XM_005274441.1:c.873A>T | XP_005274498.1:p.Glu291Asp | |
XM_011545445.1:c.873A>T | XP_011543747.1:p.Glu291Asp | |
XM_017029240.1:c.873A>T | XP_016884729.1:p.Glu291Asp | |
XM_017029241.1:c.495A>T | XP_016884730.1:p.Glu165Asp | |
NM_014271.4:c.873A>T MANE Select | NP_055086.1:p.Glu291Asp |