Canonical Allele Identifier: CA403957912

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226239T>A (hg19) ; chr19:g.10115563T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115563T>A , CM000681.2:g.10115563T>A	GRCh38
NC_000019.9:g.10226239T>A , CM000681.1:g.10226239T>A	GRCh37
NC_000019.8:g.10087239T>A	NCBI36
NG_047007.1:g.9043T>A
NG_051197.1:g.9362A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.863A>T MANE Select	ENSP00000253108.3:p.His288Leu
ENST00000253108.8:c.863A>T	ENSP00000253108.3:p.His288Leu
ENST00000589454.5:c.839A>T	ENSP00000466860.1:p.His280Leu
ENST00000590158.1:n.882A>T
ENST00000593054.5:c.257A>T	ENSP00000467187.1:p.His86Leu
NM_003755.3:c.863A>T	NP_003746.2:p.His288Leu
NM_003755.4:c.863A>T	NP_003746.2:p.His288Leu
NM_003755.5:c.863A>T MANE Select	NP_003746.2:p.His288Leu