Canonical Allele Identifier: CA403957589
Gene: EIF3G HGNC NCBI

Linked Data

gnomAD v4: 19-10115478-C-T
MyVariant Identifiers: chr19:g.10226154C>T (hg19) chr19:g.10115478C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115478C>T , CM000681.2:g.10115478C>T GRCh38
NC_000019.9:g.10226154C>T , CM000681.1:g.10226154C>T GRCh37
NC_000019.8:g.10087154C>T NCBI36
NG_047007.1:g.8958C>T
NG_051197.1:g.9447G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+1G>A MANE Select ENSP00000253108.3:n.947+1G>A
ENST00000253108.8:c.947+1G>A ENSP00000253108.3:n.947+1G>A
ENST00000590158.1:n.966+1G>A
ENST00000593054.5:c.341+1G>A ENSP00000467187.1:n.341+1G>A
NM_003755.3:c.947+1G>A NP_003746.2:n.947+1G>A
NM_003755.4:c.947+1G>A NP_003746.2:n.947+1G>A
NM_003755.5:c.947+1G>A MANE Select NP_003746.2:n.947+1G>A
Search 100 bp 5'
Search 100 bp 3'