Canonical Allele Identifier: CA9186790
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs144649796

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115511G>A , CM000681.2:g.10115511G>A GRCh38
NC_000019.9:g.10226187G>A , CM000681.1:g.10226187G>A GRCh37
NC_000019.8:g.10087187G>A NCBI36
NG_047007.1:g.8991G>A
NG_051197.1:g.9414C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.915C>T MANE Select ENSP00000253108.3:p.Tyr305=
ENST00000253108.8:c.915C>T ENSP00000253108.3:p.Tyr305=
ENST00000590158.1:n.934C>T
ENST00000593054.5:c.309C>T ENSP00000467187.1:p.Tyr103=
NM_003755.3:c.915C>T NP_003746.2:p.Tyr305=
NM_003755.4:c.915C>T NP_003746.2:p.Tyr305=
NM_003755.5:c.915C>T MANE Select NP_003746.2:p.Tyr305=