Canonical Allele Identifier: CA403957642
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115491A>C , CM000681.2:g.10115491A>C GRCh38
NC_000019.9:g.10226167A>C , CM000681.1:g.10226167A>C GRCh37
NC_000019.8:g.10087167A>C NCBI36
NG_047007.1:g.8971A>C
NG_051197.1:g.9434T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.935T>G MANE Select ENSP00000253108.3:p.Val312Gly
ENST00000253108.8:c.935T>G ENSP00000253108.3:p.Val312Gly
ENST00000590158.1:n.954T>G
ENST00000593054.5:c.329T>G ENSP00000467187.1:p.Val110Gly
NM_003755.3:c.935T>G NP_003746.2:p.Val312Gly
NM_003755.4:c.935T>G NP_003746.2:p.Val312Gly
NM_003755.5:c.935T>G MANE Select NP_003746.2:p.Val312Gly