Canonical Allele Identifier: CA505466912

Gene: EIF3G

Linked Data

• dbSNP Id: rs2145225745
• MyVariant Identifiers: chr19:g.10226223A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115547A>G , CM000681.2:g.10115547A>G	GRCh38
NC_000019.9:g.10226223A>G , CM000681.1:g.10226223A>G	GRCh37
NC_000019.8:g.10087223A>G	NCBI36
NG_047007.1:g.9027A>G
NG_051197.1:g.9378T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.879T>C MANE Select	ENSP00000253108.3:p.Ala293=
ENST00000253108.8:c.879T>C	ENSP00000253108.3:p.Ala293=
ENST00000589454.5:c.855T>C	ENSP00000466860.1:p.Ala285=
ENST00000590158.1:n.898T>C
ENST00000593054.5:c.273T>C	ENSP00000467187.1:p.Ala91=
NM_003755.3:c.879T>C	NP_003746.2:p.Ala293=
NM_003755.4:c.879T>C	NP_003746.2:p.Ala293=
NM_003755.5:c.879T>C MANE Select	NP_003746.2:p.Ala293=