Canonical Allele Identifier: CA9186817
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs751933547

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115608C>T , CM000681.2:g.10115608C>T GRCh38
NC_000019.9:g.10226284C>T , CM000681.1:g.10226284C>T GRCh37
NC_000019.8:g.10087284C>T NCBI36
NG_047007.1:g.9088C>T
NG_051197.1:g.9317G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.841-23G>A MANE Select ENSP00000253108.3:n.841-23G>A
ENST00000253108.8:c.841-23G>A ENSP00000253108.3:n.841-23G>A
ENST00000589454.5:c.817-23G>A ENSP00000466860.1:n.817-23G>A
ENST00000590158.1:n.860-23G>A
ENST00000593054.5:c.235-23G>A ENSP00000467187.1:n.235-23G>A
NM_003755.3:c.841-23G>A NP_003746.2:n.841-23G>A
NM_003755.4:c.841-23G>A NP_003746.2:n.841-23G>A
NM_003755.5:c.841-23G>A MANE Select NP_003746.2:n.841-23G>A