Canonical Allele Identifier: CA403957710

Gene: EIF3G

Linked Data

• gnomAD v4: 19-10115507-G-A
• MyVariant Identifiers: chr19:g.10226183G>A (hg19) ; chr19:g.10115507G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115507G>A , CM000681.2:g.10115507G>A	GRCh38
NC_000019.9:g.10226183G>A , CM000681.1:g.10226183G>A	GRCh37
NC_000019.8:g.10087183G>A	NCBI36
NG_047007.1:g.8987G>A
NG_051197.1:g.9418C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.919C>T MANE Select	ENSP00000253108.3:p.His307Tyr
ENST00000253108.8:c.919C>T	ENSP00000253108.3:p.His307Tyr
ENST00000590158.1:n.938C>T
ENST00000593054.5:c.313C>T	ENSP00000467187.1:p.His105Tyr
NM_003755.3:c.919C>T	NP_003746.2:p.His307Tyr
NM_003755.4:c.919C>T	NP_003746.2:p.His307Tyr
NM_003755.5:c.919C>T MANE Select	NP_003746.2:p.His307Tyr