Canonical Allele Identifier: CA2576615769
Gene: EIF3G HGNC NCBI

Linked Data

gnomAD v4: 19-10115457-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115457T>G , CM000681.2:g.10115457T>G GRCh38
NC_000019.9:g.10226133T>G , CM000681.1:g.10226133T>G GRCh37
NC_000019.8:g.10087133T>G NCBI36
NG_047007.1:g.8937T>G
NG_051197.1:g.9468A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+22A>C MANE Select ENSP00000253108.3:n.947+22A>C
ENST00000253108.8:c.947+22A>C ENSP00000253108.3:n.947+22A>C
ENST00000590158.1:n.966+22A>C
ENST00000593054.5:c.341+22A>C ENSP00000467187.1:n.341+22A>C
NM_003755.3:c.947+22A>C NP_003746.2:n.947+22A>C
NM_003755.4:c.947+22A>C NP_003746.2:n.947+22A>C
NM_003755.5:c.947+22A>C MANE Select NP_003746.2:n.947+22A>C
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