Canonical Allele Identifier: CA505466841
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs774152359
gnomAD v2: 19-10226196-G-C
MyVariant Identifiers: chr19:g.10226196G>C (hg19) chr19:g.10115520G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115520G>C , CM000681.2:g.10115520G>C GRCh38
NC_000019.9:g.10226196G>C , CM000681.1:g.10226196G>C GRCh37
NC_000019.8:g.10087196G>C NCBI36
NG_047007.1:g.9000G>C
NG_051197.1:g.9405C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.906C>G MANE Select ENSP00000253108.3:p.Gly302=
ENST00000253108.8:c.906C>G ENSP00000253108.3:p.Gly302=
ENST00000590158.1:n.925C>G
ENST00000593054.5:c.300C>G ENSP00000467187.1:p.Gly100=
NM_003755.3:c.906C>G NP_003746.2:p.Gly302=
NM_003755.4:c.906C>G NP_003746.2:p.Gly302=
NM_003755.5:c.906C>G MANE Select NP_003746.2:p.Gly302=
Search 100 bp 5'
Search 100 bp 3'