Canonical Allele Identifier: CA403957737
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115512T>G , CM000681.2:g.10115512T>G GRCh38
NC_000019.9:g.10226188T>G , CM000681.1:g.10226188T>G GRCh37
NC_000019.8:g.10087188T>G NCBI36
NG_047007.1:g.8992T>G
NG_051197.1:g.9413A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.914A>C MANE Select ENSP00000253108.3:p.Tyr305Ser
ENST00000253108.8:c.914A>C ENSP00000253108.3:p.Tyr305Ser
ENST00000590158.1:n.933A>C
ENST00000593054.5:c.308A>C ENSP00000467187.1:p.Tyr103Ser
NM_003755.3:c.914A>C NP_003746.2:p.Tyr305Ser
NM_003755.4:c.914A>C NP_003746.2:p.Tyr305Ser
NM_003755.5:c.914A>C MANE Select NP_003746.2:p.Tyr305Ser