Canonical Allele Identifier: CA505466826

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226190G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115514G>T , CM000681.2:g.10115514G>T	GRCh38
NC_000019.9:g.10226190G>T , CM000681.1:g.10226190G>T	GRCh37
NC_000019.8:g.10087190G>T	NCBI36
NG_047007.1:g.8994G>T
NG_051197.1:g.9411C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.912C>A MANE Select	ENSP00000253108.3:p.Gly304=
ENST00000253108.8:c.912C>A	ENSP00000253108.3:p.Gly304=
ENST00000590158.1:n.931C>A
ENST00000593054.5:c.306C>A	ENSP00000467187.1:p.Gly102=
NM_003755.3:c.912C>A	NP_003746.2:p.Gly304=
NM_003755.4:c.912C>A	NP_003746.2:p.Gly304=
NM_003755.5:c.912C>A MANE Select	NP_003746.2:p.Gly304=