Canonical Allele Identifier: CA505466935

Gene: EIF3G

Linked Data

• gnomAD v4: 19-10115556-G-C
• MyVariant Identifiers: chr19:g.10226232G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115556G>C , CM000681.2:g.10115556G>C	GRCh38
NC_000019.9:g.10226232G>C , CM000681.1:g.10226232G>C	GRCh37
NC_000019.8:g.10087232G>C	NCBI36
NG_047007.1:g.9036G>C
NG_051197.1:g.9369C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.870C>G MANE Select	ENSP00000253108.3:p.Arg290=
ENST00000253108.8:c.870C>G	ENSP00000253108.3:p.Arg290=
ENST00000589454.5:c.846C>G	ENSP00000466860.1:p.Arg282=
ENST00000590158.1:n.889C>G
ENST00000593054.5:c.264C>G	ENSP00000467187.1:p.Arg88=
NM_003755.3:c.870C>G	NP_003746.2:p.Arg290=
NM_003755.4:c.870C>G	NP_003746.2:p.Arg290=
NM_003755.5:c.870C>G MANE Select	NP_003746.2:p.Arg290=