Canonical Allele Identifier: CA403957813
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs2089227879
gnomAD v4: 19-10115531-C-T
MyVariant Identifiers: chr19:g.10226207C>T (hg19) chr19:g.10115531C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115531C>T , CM000681.2:g.10115531C>T GRCh38
NC_000019.9:g.10226207C>T , CM000681.1:g.10226207C>T GRCh37
NC_000019.8:g.10087207C>T NCBI36
NG_047007.1:g.9011C>T
NG_051197.1:g.9394G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.895G>A MANE Select ENSP00000253108.3:p.Gly299Arg
ENST00000253108.8:c.895G>A ENSP00000253108.3:p.Gly299Arg
ENST00000590158.1:n.914G>A
ENST00000593054.5:c.289G>A ENSP00000467187.1:p.Gly97Arg
NM_003755.3:c.895G>A NP_003746.2:p.Gly299Arg
NM_003755.4:c.895G>A NP_003746.2:p.Gly299Arg
NM_003755.5:c.895G>A MANE Select NP_003746.2:p.Gly299Arg
Search 100 bp 5'
Search 100 bp 3'