Canonical Allele Identifier: CA403957956
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1404067111

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115572A>G , CM000681.2:g.10115572A>G GRCh38
NC_000019.9:g.10226248A>G , CM000681.1:g.10226248A>G GRCh37
NC_000019.8:g.10087248A>G NCBI36
NG_047007.1:g.9052A>G
NG_051197.1:g.9353T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.854T>C MANE Select ENSP00000253108.3:p.Ile285Thr
ENST00000253108.8:c.854T>C ENSP00000253108.3:p.Ile285Thr
ENST00000589454.5:c.830T>C ENSP00000466860.1:p.Ile277Thr
ENST00000590158.1:n.873T>C
ENST00000593054.5:c.248T>C ENSP00000467187.1:p.Ile83Thr
NM_003755.3:c.854T>C NP_003746.2:p.Ile285Thr
NM_003755.4:c.854T>C NP_003746.2:p.Ile285Thr
NM_003755.5:c.854T>C MANE Select NP_003746.2:p.Ile285Thr