Canonical Allele Identifier: CA403957681

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226176A>G (hg19) ; chr19:g.10115500A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115500A>G , CM000681.2:g.10115500A>G	GRCh38
NC_000019.9:g.10226176A>G , CM000681.1:g.10226176A>G	GRCh37
NC_000019.8:g.10087176A>G	NCBI36
NG_047007.1:g.8980A>G
NG_051197.1:g.9425T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.926T>C MANE Select	ENSP00000253108.3:p.Ile309Thr
ENST00000253108.8:c.926T>C	ENSP00000253108.3:p.Ile309Thr
ENST00000590158.1:n.945T>C
ENST00000593054.5:c.320T>C	ENSP00000467187.1:p.Ile107Thr
NM_003755.3:c.926T>C	NP_003746.2:p.Ile309Thr
NM_003755.4:c.926T>C	NP_003746.2:p.Ile309Thr
NM_003755.5:c.926T>C MANE Select	NP_003746.2:p.Ile309Thr