HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154034T>C , CM000681.2:g.55154034T>C | GRCh38 |
NC_000019.9:g.55665402T>C , CM000681.1:g.55665402T>C | GRCh37 |
NC_000019.8:g.60357214T>C | NCBI36 |
NG_007866.2:g.8699A>G , LRG_432:g.8699A>G | |
NG_011829.2:g.205A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.545A>G MANE Select | ENSP00000341838.5:p.Glu182Gly | |
ENST00000665070.1:c.578A>G | ENSP00000499482.1:p.Glu193Gly | |
ENST00000344887.9:c.545A>G | ENSP00000341838.5:p.Glu182Gly | |
ENST00000585806.5:n.544A>G | ||
ENST00000588882.1:c.470A>G | ENSP00000466729.1:p.Glu157Gly | |
ENST00000589864.1:n.373A>G | ||
NM_000363.4:c.545A>G , LRG_432t1:c.545A>G | NP_000354.4:p.Glu182Gly | |
NM_000363.5:c.545A>G MANE Select | NP_000354.4:p.Glu182Gly |