Canonical Allele Identifier: CA631709094
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1402452462
gnomAD v2: 19-10226314-A-G
gnomAD v4: 19-10115638-A-G
MyVariant Identifiers: chr19:g.10226314A>G (hg19) chr19:g.10115638A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115638A>G , CM000681.2:g.10115638A>G GRCh38
NC_000019.9:g.10226314A>G , CM000681.1:g.10226314A>G GRCh37
NC_000019.8:g.10087314A>G NCBI36
NG_047007.1:g.9118A>G
NG_051197.1:g.9287T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+46T>C MANE Select ENSP00000253108.3:n.840+46T>C
ENST00000253108.8:c.840+46T>C ENSP00000253108.3:n.840+46T>C
ENST00000589454.5:c.816+46T>C ENSP00000466860.1:n.816+46T>C
ENST00000590158.1:n.859+46T>C
ENST00000593054.5:c.234+46T>C ENSP00000467187.1:n.234+46T>C
NM_003755.3:c.840+46T>C NP_003746.2:n.840+46T>C
NM_003755.4:c.840+46T>C NP_003746.2:n.840+46T>C
NM_003755.5:c.840+46T>C MANE Select NP_003746.2:n.840+46T>C
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