Canonical Allele Identifier: CA403957942

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226245C>G (hg19) ; chr19:g.10115569C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115569C>G , CM000681.2:g.10115569C>G	GRCh38
NC_000019.9:g.10226245C>G , CM000681.1:g.10226245C>G	GRCh37
NC_000019.8:g.10087245C>G	NCBI36
NG_047007.1:g.9049C>G
NG_051197.1:g.9356G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.857G>C MANE Select	ENSP00000253108.3:p.Ser286Thr
ENST00000253108.8:c.857G>C	ENSP00000253108.3:p.Ser286Thr
ENST00000589454.5:c.833G>C	ENSP00000466860.1:p.Ser278Thr
ENST00000590158.1:n.876G>C
ENST00000593054.5:c.251G>C	ENSP00000467187.1:p.Ser84Thr
NM_003755.3:c.857G>C	NP_003746.2:p.Ser286Thr
NM_003755.4:c.857G>C	NP_003746.2:p.Ser286Thr
NM_003755.5:c.857G>C MANE Select	NP_003746.2:p.Ser286Thr