Canonical Allele Identifier: CA505466793
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1378625861
gnomAD v2: 19-10226178-G-A
gnomAD v4: 19-10115502-G-A
MyVariant Identifiers: chr19:g.10226178G>A (hg19) chr19:g.10115502G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115502G>A , CM000681.2:g.10115502G>A GRCh38
NC_000019.9:g.10226178G>A , CM000681.1:g.10226178G>A GRCh37
NC_000019.8:g.10087178G>A NCBI36
NG_047007.1:g.8982G>A
NG_051197.1:g.9423C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.924C>T MANE Select ENSP00000253108.3:p.Leu308=
ENST00000253108.8:c.924C>T ENSP00000253108.3:p.Leu308=
ENST00000590158.1:n.943C>T
ENST00000593054.5:c.318C>T ENSP00000467187.1:p.Leu106=
NM_003755.3:c.924C>T NP_003746.2:p.Leu308=
NM_003755.4:c.924C>T NP_003746.2:p.Leu308=
NM_003755.5:c.924C>T MANE Select NP_003746.2:p.Leu308=
Search 100 bp 5'
Search 100 bp 3'