Canonical Allele Identifier: CA403957647

Gene: EIF3G

Linked Data

• gnomAD v4: 19-10115492-C-A
• MyVariant Identifiers: chr19:g.10226168C>A (hg19) ; chr19:g.10115492C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115492C>A , CM000681.2:g.10115492C>A	GRCh38
NC_000019.9:g.10226168C>A , CM000681.1:g.10226168C>A	GRCh37
NC_000019.8:g.10087168C>A	NCBI36
NG_047007.1:g.8972C>A
NG_051197.1:g.9433G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.934G>T MANE Select	ENSP00000253108.3:p.Val312Phe
ENST00000253108.8:c.934G>T	ENSP00000253108.3:p.Val312Phe
ENST00000590158.1:n.953G>T
ENST00000593054.5:c.328G>T	ENSP00000467187.1:p.Val110Phe
NM_003755.3:c.934G>T	NP_003746.2:p.Val312Phe
NM_003755.4:c.934G>T	NP_003746.2:p.Val312Phe
NM_003755.5:c.934G>T MANE Select	NP_003746.2:p.Val312Phe