Canonical Allele Identifier: CA9186839
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs753028203
ExAC: 19:10226335 C / G
gnomAD v2: 19-10226335-C-G
gnomAD v4: 19-10115659-C-G
MyVariant Identifiers: chr19:g.10226335C>G (hg19) chr19:g.10115659C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115659C>G , CM000681.2:g.10115659C>G GRCh38
NC_000019.9:g.10226335C>G , CM000681.1:g.10226335C>G GRCh37
NC_000019.8:g.10087335C>G NCBI36
NG_047007.1:g.9139C>G
NG_051197.1:g.9266G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+25G>C MANE Select ENSP00000253108.3:n.840+25G>C
ENST00000253108.8:c.840+25G>C ENSP00000253108.3:n.840+25G>C
ENST00000589454.5:c.816+25G>C ENSP00000466860.1:n.816+25G>C
ENST00000590158.1:n.859+25G>C
ENST00000593054.5:c.234+25G>C ENSP00000467187.1:n.234+25G>C
NM_003755.3:c.840+25G>C NP_003746.2:n.840+25G>C
NM_003755.4:c.840+25G>C NP_003746.2:n.840+25G>C
NM_003755.5:c.840+25G>C MANE Select NP_003746.2:n.840+25G>C
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