Canonical Allele Identifier: CA631709062
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs765829507
gnomAD v2: 19-10226140-G-C
gnomAD v4: 19-10115464-G-C
MyVariant Identifiers: chr19:g.10226140G>C (hg19) chr19:g.10115464G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115464G>C , CM000681.2:g.10115464G>C GRCh38
NC_000019.9:g.10226140G>C , CM000681.1:g.10226140G>C GRCh37
NC_000019.8:g.10087140G>C NCBI36
NG_047007.1:g.8944G>C
NG_051197.1:g.9461C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+15C>G MANE Select ENSP00000253108.3:n.947+15C>G
ENST00000253108.8:c.947+15C>G ENSP00000253108.3:n.947+15C>G
ENST00000590158.1:n.966+15C>G
ENST00000593054.5:c.341+15C>G ENSP00000467187.1:n.341+15C>G
NM_003755.3:c.947+15C>G NP_003746.2:n.947+15C>G
NM_003755.4:c.947+15C>G NP_003746.2:n.947+15C>G
NM_003755.5:c.947+15C>G MANE Select NP_003746.2:n.947+15C>G
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