Canonical Allele Identifier: CA631709063
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1239346177
gnomAD v2: 19-10226150-C-A
gnomAD v4: 19-10115474-C-A
MyVariant Identifiers: chr19:g.10226150C>A (hg19) chr19:g.10115474C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115474C>A , CM000681.2:g.10115474C>A GRCh38
NC_000019.9:g.10226150C>A , CM000681.1:g.10226150C>A GRCh37
NC_000019.8:g.10087150C>A NCBI36
NG_047007.1:g.8954C>A
NG_051197.1:g.9451G>T

Transcript Alleles

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