Canonical Allele Identifier: CA783165837
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1340516767

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115452G>A , CM000681.2:g.10115452G>A GRCh38
NC_000019.9:g.10226128G>A , CM000681.1:g.10226128G>A GRCh37
NC_000019.8:g.10087128G>A NCBI36
NG_047007.1:g.8932G>A
NG_051197.1:g.9473C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+27C>T MANE Select ENSP00000253108.3:n.947+27C>T
ENST00000253108.8:c.947+27C>T ENSP00000253108.3:n.947+27C>T
ENST00000590158.1:n.966+27C>T
ENST00000593054.5:c.341+27C>T ENSP00000467187.1:n.341+27C>T
NM_003755.3:c.947+27C>T NP_003746.2:n.947+27C>T
NM_003755.4:c.947+27C>T NP_003746.2:n.947+27C>T
NM_003755.5:c.947+27C>T MANE Select NP_003746.2:n.947+27C>T