Canonical Allele Identifier: CA9186780
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs376608627

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115468T>C , CM000681.2:g.10115468T>C GRCh38
NC_000019.9:g.10226144T>C , CM000681.1:g.10226144T>C GRCh37
NC_000019.8:g.10087144T>C NCBI36
NG_047007.1:g.8948T>C
NG_051197.1:g.9457A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+11A>G MANE Select ENSP00000253108.3:n.947+11A>G
ENST00000253108.8:c.947+11A>G ENSP00000253108.3:n.947+11A>G
ENST00000590158.1:n.966+11A>G
ENST00000593054.5:c.341+11A>G ENSP00000467187.1:n.341+11A>G
NM_003755.3:c.947+11A>G NP_003746.2:n.947+11A>G
NM_003755.4:c.947+11A>G NP_003746.2:n.947+11A>G
NM_003755.5:c.947+11A>G MANE Select NP_003746.2:n.947+11A>G