Canonical Allele Identifier: CA403957876
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226229C>G (hg19) chr19:g.10115553C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115553C>G , CM000681.2:g.10115553C>G GRCh38
NC_000019.9:g.10226229C>G , CM000681.1:g.10226229C>G GRCh37
NC_000019.8:g.10087229C>G NCBI36
NG_047007.1:g.9033C>G
NG_051197.1:g.9372G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.873G>C MANE Select ENSP00000253108.3:p.Glu291Asp
ENST00000253108.8:c.873G>C ENSP00000253108.3:p.Glu291Asp
ENST00000589454.5:c.849G>C ENSP00000466860.1:p.Glu283Asp
ENST00000590158.1:n.892G>C
ENST00000593054.5:c.267G>C ENSP00000467187.1:p.Glu89Asp
NM_003755.3:c.873G>C NP_003746.2:p.Glu291Asp
NM_003755.4:c.873G>C NP_003746.2:p.Glu291Asp
NM_003755.5:c.873G>C MANE Select NP_003746.2:p.Glu291Asp
Search 100 bp 5'
Search 100 bp 3'