Canonical Allele Identifier: CA9186776
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs200086408

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115448A>G , CM000681.2:g.10115448A>G GRCh38
NC_000019.9:g.10226124A>G , CM000681.1:g.10226124A>G GRCh37
NC_000019.8:g.10087124A>G NCBI36
NG_047007.1:g.8928A>G
NG_051197.1:g.9477T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+31T>C MANE Select ENSP00000253108.3:n.947+31T>C
ENST00000253108.8:c.947+31T>C ENSP00000253108.3:n.947+31T>C
ENST00000590158.1:n.966+31T>C
ENST00000593054.5:c.341+31T>C ENSP00000467187.1:n.341+31T>C
NM_003755.3:c.947+31T>C NP_003746.2:n.947+31T>C
NM_003755.4:c.947+31T>C NP_003746.2:n.947+31T>C
NM_003755.5:c.947+31T>C MANE Select NP_003746.2:n.947+31T>C