Canonical Allele Identifier: CA403957672

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226174G>C (hg19) ; chr19:g.10115498G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115498G>C , CM000681.2:g.10115498G>C	GRCh38
NC_000019.9:g.10226174G>C , CM000681.1:g.10226174G>C	GRCh37
NC_000019.8:g.10087174G>C	NCBI36
NG_047007.1:g.8978G>C
NG_051197.1:g.9427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.928C>G MANE Select	ENSP00000253108.3:p.Leu310Val
ENST00000253108.8:c.928C>G	ENSP00000253108.3:p.Leu310Val
ENST00000590158.1:n.947C>G
ENST00000593054.5:c.322C>G	ENSP00000467187.1:p.Leu108Val
NM_003755.3:c.928C>G	NP_003746.2:p.Leu310Val
NM_003755.4:c.928C>G	NP_003746.2:p.Leu310Val
NM_003755.5:c.928C>G MANE Select	NP_003746.2:p.Leu310Val