Canonical Allele Identifier: CA403957894
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1481001310

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115558G>A , CM000681.2:g.10115558G>A GRCh38
NC_000019.9:g.10226234G>A , CM000681.1:g.10226234G>A GRCh37
NC_000019.8:g.10087234G>A NCBI36
NG_047007.1:g.9038G>A
NG_051197.1:g.9367C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.868C>T MANE Select ENSP00000253108.3:p.Arg290Cys
ENST00000253108.8:c.868C>T ENSP00000253108.3:p.Arg290Cys
ENST00000589454.5:c.844C>T ENSP00000466860.1:p.Arg282Cys
ENST00000590158.1:n.887C>T
ENST00000593054.5:c.262C>T ENSP00000467187.1:p.Arg88Cys
NM_003755.3:c.868C>T NP_003746.2:p.Arg290Cys
NM_003755.4:c.868C>T NP_003746.2:p.Arg290Cys
NM_003755.5:c.868C>T MANE Select NP_003746.2:p.Arg290Cys