Canonical Allele Identifier: CA9186803
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs747730661
ExAC: 19:10226241 G / C
gnomAD v2: 19-10226241-G-C
gnomAD v4: 19-10115565-G-C
MyVariant Identifiers: chr19:g.10226241G>C (hg19) chr19:g.10115565G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115565G>C , CM000681.2:g.10115565G>C GRCh38
NC_000019.9:g.10226241G>C , CM000681.1:g.10226241G>C GRCh37
NC_000019.8:g.10087241G>C NCBI36
NG_047007.1:g.9045G>C
NG_051197.1:g.9360C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.861C>G MANE Select ENSP00000253108.3:p.Phe287Leu
ENST00000253108.8:c.861C>G ENSP00000253108.3:p.Phe287Leu
ENST00000589454.5:c.837C>G ENSP00000466860.1:p.Phe279Leu
ENST00000590158.1:n.880C>G
ENST00000593054.5:c.255C>G ENSP00000467187.1:p.Phe85Leu
NM_003755.3:c.861C>G NP_003746.2:p.Phe287Leu
NM_003755.4:c.861C>G NP_003746.2:p.Phe287Leu
NM_003755.5:c.861C>G MANE Select NP_003746.2:p.Phe287Leu
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