Canonical Allele Identifier: CA9186813
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs770016640

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115598G>A , CM000681.2:g.10115598G>A GRCh38
NC_000019.9:g.10226274G>A , CM000681.1:g.10226274G>A GRCh37
NC_000019.8:g.10087274G>A NCBI36
NG_047007.1:g.9078G>A
NG_051197.1:g.9327C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.841-13C>T MANE Select ENSP00000253108.3:n.841-13C>T
ENST00000253108.8:c.841-13C>T ENSP00000253108.3:n.841-13C>T
ENST00000589454.5:c.817-13C>T ENSP00000466860.1:n.817-13C>T
ENST00000590158.1:n.860-13C>T
ENST00000593054.5:c.235-13C>T ENSP00000467187.1:n.235-13C>T
NM_003755.3:c.841-13C>T NP_003746.2:n.841-13C>T
NM_003755.4:c.841-13C>T NP_003746.2:n.841-13C>T
NM_003755.5:c.841-13C>T MANE Select NP_003746.2:n.841-13C>T