Canonical Allele Identifier: CA631709096
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1276803540
gnomAD v2: 19-10226315-C-G
gnomAD v4: 19-10115639-C-G
MyVariant Identifiers: chr19:g.10226315C>G (hg19) chr19:g.10115639C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115639C>G , CM000681.2:g.10115639C>G GRCh38
NC_000019.9:g.10226315C>G , CM000681.1:g.10226315C>G GRCh37
NC_000019.8:g.10087315C>G NCBI36
NG_047007.1:g.9119C>G
NG_051197.1:g.9286G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+45G>C MANE Select ENSP00000253108.3:n.840+45G>C
ENST00000253108.8:c.840+45G>C ENSP00000253108.3:n.840+45G>C
ENST00000589454.5:c.816+45G>C ENSP00000466860.1:n.816+45G>C
ENST00000590158.1:n.859+45G>C
ENST00000593054.5:c.234+45G>C ENSP00000467187.1:n.234+45G>C
NM_003755.3:c.840+45G>C NP_003746.2:n.840+45G>C
NM_003755.4:c.840+45G>C NP_003746.2:n.840+45G>C
NM_003755.5:c.840+45G>C MANE Select NP_003746.2:n.840+45G>C
Search 100 bp 5'
Search 100 bp 3'