Canonical Allele Identifier: CA403957779
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226198C>T (hg19) chr19:g.10115522C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115522C>T , CM000681.2:g.10115522C>T GRCh38
NC_000019.9:g.10226198C>T , CM000681.1:g.10226198C>T GRCh37
NC_000019.8:g.10087198C>T NCBI36
NG_047007.1:g.9002C>T
NG_051197.1:g.9403G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.904G>A MANE Select ENSP00000253108.3:p.Gly302Ser
ENST00000253108.8:c.904G>A ENSP00000253108.3:p.Gly302Ser
ENST00000590158.1:n.923G>A
ENST00000593054.5:c.298G>A ENSP00000467187.1:p.Gly100Ser
NM_003755.3:c.904G>A NP_003746.2:p.Gly302Ser
NM_003755.4:c.904G>A NP_003746.2:p.Gly302Ser
NM_003755.5:c.904G>A MANE Select NP_003746.2:p.Gly302Ser
Search 100 bp 5'
Search 100 bp 3'