Canonical Allele Identifier: CA631709060
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1362239462
gnomAD v2: 19-10226134-G-A
gnomAD v4: 19-10115458-G-A
MyVariant Identifiers: chr19:g.10226134G>A (hg19) chr19:g.10115458G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115458G>A , CM000681.2:g.10115458G>A GRCh38
NC_000019.9:g.10226134G>A , CM000681.1:g.10226134G>A GRCh37
NC_000019.8:g.10087134G>A NCBI36
NG_047007.1:g.8938G>A
NG_051197.1:g.9467C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+21C>T MANE Select ENSP00000253108.3:n.947+21C>T
ENST00000253108.8:c.947+21C>T ENSP00000253108.3:n.947+21C>T
ENST00000590158.1:n.966+21C>T
ENST00000593054.5:c.341+21C>T ENSP00000467187.1:n.341+21C>T
NM_003755.3:c.947+21C>T NP_003746.2:n.947+21C>T
NM_003755.4:c.947+21C>T NP_003746.2:n.947+21C>T
NM_003755.5:c.947+21C>T MANE Select NP_003746.2:n.947+21C>T
Search 100 bp 5'
Search 100 bp 3'