Canonical Allele Identifier: CA505466866
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226205C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115529C>G , CM000681.2:g.10115529C>G GRCh38
NC_000019.9:g.10226205C>G , CM000681.1:g.10226205C>G GRCh37
NC_000019.8:g.10087205C>G NCBI36
NG_047007.1:g.9009C>G
NG_051197.1:g.9396G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.897G>C MANE Select ENSP00000253108.3:p.Gly299=
ENST00000253108.8:c.897G>C ENSP00000253108.3:p.Gly299=
ENST00000590158.1:n.916G>C
ENST00000593054.5:c.291G>C ENSP00000467187.1:p.Gly97=
NM_003755.3:c.897G>C NP_003746.2:p.Gly299=
NM_003755.4:c.897G>C NP_003746.2:p.Gly299=
NM_003755.5:c.897G>C MANE Select NP_003746.2:p.Gly299=