Canonical Allele Identifier: CA403957627
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226162A>T (hg19) chr19:g.10115486A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115486A>T , CM000681.2:g.10115486A>T GRCh38
NC_000019.9:g.10226162A>T , CM000681.1:g.10226162A>T GRCh37
NC_000019.8:g.10087162A>T NCBI36
NG_047007.1:g.8966A>T
NG_051197.1:g.9439T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.940T>A MANE Select ENSP00000253108.3:p.Trp314Arg
ENST00000253108.8:c.940T>A ENSP00000253108.3:p.Trp314Arg
ENST00000590158.1:n.959T>A
ENST00000593054.5:c.334T>A ENSP00000467187.1:p.Trp112Arg
NM_003755.3:c.940T>A NP_003746.2:p.Trp314Arg
NM_003755.4:c.940T>A NP_003746.2:p.Trp314Arg
NM_003755.5:c.940T>A MANE Select NP_003746.2:p.Trp314Arg
Search 100 bp 5'
Search 100 bp 3'