Canonical Allele Identifier: CA9186783
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs746664456

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115476T>C , CM000681.2:g.10115476T>C GRCh38
NC_000019.9:g.10226152T>C , CM000681.1:g.10226152T>C GRCh37
NC_000019.8:g.10087152T>C NCBI36
NG_047007.1:g.8956T>C
NG_051197.1:g.9449A>G

Transcript Alleles

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