HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845365A>G , CM000685.2:g.21845365A>G | GRCh38 |
NC_000023.10:g.21863483A>G , CM000685.1:g.21863483A>G | GRCh37 |
NC_000023.9:g.21773404A>G | NCBI36 |
NG_012797.1:g.10828A>G | |
NG_012797.2:g.10828A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.419A>G MANE Select | ENSP00000368798.5:p.Glu140Gly | |
ENST00000365779.2:c.419A>G | ENSP00000368796.1:p.Glu140Gly | |
ENST00000379484.9:c.419A>G | ENSP00000368798.5:p.Glu140Gly | |
ENST00000465888.1:n.518A>G | ||
NM_015884.3:c.419A>G | NP_056968.1:p.Glu140Gly | |
NM_015884.4:c.419A>G MANE Select | NP_056968.1:p.Glu140Gly |