Canonical Allele Identifier: CA9186830
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs549483404
ExAC: 19:10226312 G / T
gnomAD v2: 19-10226312-G-T
gnomAD v3: 19-10115636-G-T
gnomAD v4: 19-10115636-G-T
MyVariant Identifiers: chr19:g.10226312G>T (hg19) chr19:g.10115636G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115636G>T , CM000681.2:g.10115636G>T GRCh38
NC_000019.9:g.10226312G>T , CM000681.1:g.10226312G>T GRCh37
NC_000019.8:g.10087312G>T NCBI36
NG_047007.1:g.9116G>T
NG_051197.1:g.9289C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+48C>A MANE Select ENSP00000253108.3:n.840+48C>A
ENST00000253108.8:c.840+48C>A ENSP00000253108.3:n.840+48C>A
ENST00000589454.5:c.816+48C>A ENSP00000466860.1:n.816+48C>A
ENST00000590158.1:n.859+48C>A
ENST00000593054.5:c.234+48C>A ENSP00000467187.1:n.234+48C>A
NM_003755.3:c.840+48C>A NP_003746.2:n.840+48C>A
NM_003755.4:c.840+48C>A NP_003746.2:n.840+48C>A
NM_003755.5:c.840+48C>A MANE Select NP_003746.2:n.840+48C>A
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