Canonical Allele Identifier: CA505466902

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226217A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115541A>C , CM000681.2:g.10115541A>C	GRCh38
NC_000019.9:g.10226217A>C , CM000681.1:g.10226217A>C	GRCh37
NC_000019.8:g.10087217A>C	NCBI36
NG_047007.1:g.9021A>C
NG_051197.1:g.9384T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.885T>G MANE Select	ENSP00000253108.3:p.Arg295=
ENST00000253108.8:c.885T>G	ENSP00000253108.3:p.Arg295=
ENST00000589454.5:c.861T>G	ENSP00000466860.1:p.Arg287=
ENST00000590158.1:n.904T>G
ENST00000593054.5:c.279T>G	ENSP00000467187.1:p.Arg93=
NM_003755.3:c.885T>G	NP_003746.2:p.Arg295=
NM_003755.4:c.885T>G	NP_003746.2:p.Arg295=
NM_003755.5:c.885T>G MANE Select	NP_003746.2:p.Arg295=