Canonical Allele Identifier: CA9186795
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs761983718
ExAC: 19:10226220 C / T
gnomAD v2: 19-10226220-C-T
gnomAD v3: 19-10115544-C-T
gnomAD v4: 19-10115544-C-T
MyVariant Identifiers: chr19:g.10226220C>T (hg19) chr19:g.10115544C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115544C>T , CM000681.2:g.10115544C>T GRCh38
NC_000019.9:g.10226220C>T , CM000681.1:g.10226220C>T GRCh37
NC_000019.8:g.10087220C>T NCBI36
NG_047007.1:g.9024C>T
NG_051197.1:g.9381G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.882G>A MANE Select ENSP00000253108.3:p.Ala294=
ENST00000253108.8:c.882G>A ENSP00000253108.3:p.Ala294=
ENST00000589454.5:c.858G>A ENSP00000466860.1:p.Ala286=
ENST00000590158.1:n.901G>A
ENST00000593054.5:c.276G>A ENSP00000467187.1:p.Ala92=
NM_003755.3:c.882G>A NP_003746.2:p.Ala294=
NM_003755.4:c.882G>A NP_003746.2:p.Ala294=
NM_003755.5:c.882G>A MANE Select NP_003746.2:p.Ala294=
Search 100 bp 5'
Search 100 bp 3'