Canonical Allele Identifier: CA2322270290
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs369537875

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115469G>A , CM000681.2:g.10115469G>A GRCh38
NC_000019.9:g.10226145G>A , CM000681.1:g.10226145G>A GRCh37
NC_000019.8:g.10087145G>A NCBI36
NG_047007.1:g.8949G>A
NG_051197.1:g.9456C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+10C>T MANE Select ENSP00000253108.3:n.947+10C>T
ENST00000253108.8:c.947+10C>T ENSP00000253108.3:n.947+10C>T
ENST00000590158.1:n.966+10C>T
ENST00000593054.5:c.341+10C>T ENSP00000467187.1:n.341+10C>T
NM_003755.3:c.947+10C>T NP_003746.2:n.947+10C>T
NM_003755.4:c.947+10C>T NP_003746.2:n.947+10C>T
NM_003755.5:c.947+10C>T MANE Select NP_003746.2:n.947+10C>T