Canonical Allele Identifier: CA403957767
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226195A>C (hg19) chr19:g.10115519A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115519A>C , CM000681.2:g.10115519A>C GRCh38
NC_000019.9:g.10226195A>C , CM000681.1:g.10226195A>C GRCh37
NC_000019.8:g.10087195A>C NCBI36
NG_047007.1:g.8999A>C
NG_051197.1:g.9406T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.907T>G MANE Select ENSP00000253108.3:p.Phe303Val
ENST00000253108.8:c.907T>G ENSP00000253108.3:p.Phe303Val
ENST00000590158.1:n.926T>G
ENST00000593054.5:c.301T>G ENSP00000467187.1:p.Phe101Val
NM_003755.3:c.907T>G NP_003746.2:p.Phe303Val
NM_003755.4:c.907T>G NP_003746.2:p.Phe303Val
NM_003755.5:c.907T>G MANE Select NP_003746.2:p.Phe303Val
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Search 100 bp 3'