Canonical Allele Identifier: CA2322270287
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1599324531
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115467A>G , CM000681.2:g.10115467A>G GRCh38
NC_000019.9:g.10226143A>G , CM000681.1:g.10226143A>G GRCh37
NC_000019.8:g.10087143A>G NCBI36
NG_047007.1:g.8947A>G
NG_051197.1:g.9458T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+12T>C MANE Select ENSP00000253108.3:n.947+12T>C
ENST00000253108.8:c.947+12T>C ENSP00000253108.3:n.947+12T>C
ENST00000590158.1:n.966+12T>C
ENST00000593054.5:c.341+12T>C ENSP00000467187.1:n.341+12T>C
NM_003755.3:c.947+12T>C NP_003746.2:n.947+12T>C
NM_003755.4:c.947+12T>C NP_003746.2:n.947+12T>C
NM_003755.5:c.947+12T>C MANE Select NP_003746.2:n.947+12T>C
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