Canonical Allele Identifier: CA505466800
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226181G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115505G>A , CM000681.2:g.10115505G>A GRCh38
NC_000019.9:g.10226181G>A , CM000681.1:g.10226181G>A GRCh37
NC_000019.8:g.10087181G>A NCBI36
NG_047007.1:g.8985G>A
NG_051197.1:g.9420C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.921C>T MANE Select ENSP00000253108.3:p.His307=
ENST00000253108.8:c.921C>T ENSP00000253108.3:p.His307=
ENST00000590158.1:n.940C>T
ENST00000593054.5:c.315C>T ENSP00000467187.1:p.His105=
NM_003755.3:c.921C>T NP_003746.2:p.His307=
NM_003755.4:c.921C>T NP_003746.2:p.His307=
NM_003755.5:c.921C>T MANE Select NP_003746.2:p.His307=