Canonical Allele Identifier: CA403957976
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226252A>C (hg19) chr19:g.10115576A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115576A>C , CM000681.2:g.10115576A>C GRCh38
NC_000019.9:g.10226252A>C , CM000681.1:g.10226252A>C GRCh37
NC_000019.8:g.10087252A>C NCBI36
NG_047007.1:g.9056A>C
NG_051197.1:g.9349T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.850T>G MANE Select ENSP00000253108.3:p.Phe284Val
ENST00000253108.8:c.850T>G ENSP00000253108.3:p.Phe284Val
ENST00000589454.5:c.826T>G ENSP00000466860.1:p.Phe276Val
ENST00000590158.1:n.869T>G
ENST00000593054.5:c.244T>G ENSP00000467187.1:p.Phe82Val
NM_003755.3:c.850T>G NP_003746.2:p.Phe284Val
NM_003755.4:c.850T>G NP_003746.2:p.Phe284Val
NM_003755.5:c.850T>G MANE Select NP_003746.2:p.Phe284Val
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