Canonical Allele Identifier: CA783165833
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1281949957
gnomAD v3: 19-10115437-A-C
gnomAD v4: 19-10115437-A-C
MyVariant Identifiers: chr19:g.10226113A>C (hg19) chr19:g.10115437A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115437A>C , CM000681.2:g.10115437A>C GRCh38
NC_000019.9:g.10226113A>C , CM000681.1:g.10226113A>C GRCh37
NC_000019.8:g.10087113A>C NCBI36
NG_047007.1:g.8917A>C
NG_051197.1:g.9488T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+42T>G MANE Select ENSP00000253108.3:n.947+42T>G
ENST00000253108.8:c.947+42T>G ENSP00000253108.3:n.947+42T>G
ENST00000590158.1:n.966+42T>G
ENST00000593054.5:c.341+42T>G ENSP00000467187.1:n.341+42T>G
NM_003755.3:c.947+42T>G NP_003746.2:n.947+42T>G
NM_003755.4:c.947+42T>G NP_003746.2:n.947+42T>G
NM_003755.5:c.947+42T>G MANE Select NP_003746.2:n.947+42T>G
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