HGVS | Genome Assembly |
---|---|
NC_000001.11:g.67053939A>T , CM000663.2:g.67053939A>T | GRCh38 |
NC_000001.10:g.67519622A>T , CM000663.1:g.67519622A>T | GRCh37 |
NC_000001.9:g.67292210A>T | NCBI36 |
NG_012933.1:g.5459T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000235345.6:c.75T>A MANE Select | ENSP00000235345.5:p.Asp25Glu | |
ENST00000235345.5:c.75T>A | ENSP00000235345.5:p.Asp25Glu | |
NM_015139.2:c.75T>A | NP_055954.1:p.Asp25Glu | |
XM_006710478.1:c.75T>A | XP_006710541.1:p.Asp25Glu | |
XM_011541070.1:c.75T>A | XP_011539372.1:p.Asp25Glu | |
XM_006710478.2:c.75T>A | XP_006710541.1:p.Asp25Glu | |
XM_011541070.2:c.75T>A | XP_011539372.1:p.Asp25Glu | |
XR_001737057.2:n.485T>A | ||
XR_001737058.2:n.478T>A | ||
NM_015139.3:c.75T>A MANE Select | NP_055954.1:p.Asp25Glu |