Canonical Allele Identifier: CA505466887
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226211A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115535A>T , CM000681.2:g.10115535A>T GRCh38
NC_000019.9:g.10226211A>T , CM000681.1:g.10226211A>T GRCh37
NC_000019.8:g.10087211A>T NCBI36
NG_047007.1:g.9015A>T
NG_051197.1:g.9390T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.891T>A MANE Select ENSP00000253108.3:p.Ile297=
ENST00000253108.8:c.891T>A ENSP00000253108.3:p.Ile297=
ENST00000589454.5:c.867T>A ENSP00000466860.1:p.Ile289=
ENST00000590158.1:n.910T>A
ENST00000593054.5:c.285T>A ENSP00000467187.1:p.Ile95=
NM_003755.3:c.891T>A NP_003746.2:p.Ile297=
NM_003755.4:c.891T>A NP_003746.2:p.Ile297=
NM_003755.5:c.891T>A MANE Select NP_003746.2:p.Ile297=