Canonical Allele Identifier: CA2588321582
Gene: EIF3G HGNC NCBI

Linked Data

gnomAD v4: 19-10115611-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115611G>C , CM000681.2:g.10115611G>C GRCh38
NC_000019.9:g.10226287G>C , CM000681.1:g.10226287G>C GRCh37
NC_000019.8:g.10087287G>C NCBI36
NG_047007.1:g.9091G>C
NG_051197.1:g.9314C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.841-26C>G MANE Select ENSP00000253108.3:n.841-26C>G
ENST00000253108.8:c.841-26C>G ENSP00000253108.3:n.841-26C>G
ENST00000589454.5:c.817-26C>G ENSP00000466860.1:n.817-26C>G
ENST00000590158.1:n.860-26C>G
ENST00000593054.5:c.235-26C>G ENSP00000467187.1:n.235-26C>G
NM_003755.3:c.841-26C>G NP_003746.2:n.841-26C>G
NM_003755.4:c.841-26C>G NP_003746.2:n.841-26C>G
NM_003755.5:c.841-26C>G MANE Select NP_003746.2:n.841-26C>G
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