Canonical Allele Identifier: CA2588321583
Gene: EIF3G HGNC NCBI

Linked Data

gnomAD v4: 19-10115614-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115614C>G , CM000681.2:g.10115614C>G GRCh38
NC_000019.9:g.10226290C>G , CM000681.1:g.10226290C>G GRCh37
NC_000019.8:g.10087290C>G NCBI36
NG_047007.1:g.9094C>G
NG_051197.1:g.9311G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.841-29G>C MANE Select ENSP00000253108.3:n.841-29G>C
ENST00000253108.8:c.841-29G>C ENSP00000253108.3:n.841-29G>C
ENST00000589454.5:c.817-29G>C ENSP00000466860.1:n.817-29G>C
ENST00000590158.1:n.860-29G>C
ENST00000593054.5:c.235-29G>C ENSP00000467187.1:n.235-29G>C
NM_003755.3:c.841-29G>C NP_003746.2:n.841-29G>C
NM_003755.4:c.841-29G>C NP_003746.2:n.841-29G>C
NM_003755.5:c.841-29G>C MANE Select NP_003746.2:n.841-29G>C
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