Canonical Allele Identifier: CA403957741
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226189A>G (hg19) chr19:g.10115513A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115513A>G , CM000681.2:g.10115513A>G GRCh38
NC_000019.9:g.10226189A>G , CM000681.1:g.10226189A>G GRCh37
NC_000019.8:g.10087189A>G NCBI36
NG_047007.1:g.8993A>G
NG_051197.1:g.9412T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.913T>C MANE Select ENSP00000253108.3:p.Tyr305His
ENST00000253108.8:c.913T>C ENSP00000253108.3:p.Tyr305His
ENST00000590158.1:n.932T>C
ENST00000593054.5:c.307T>C ENSP00000467187.1:p.Tyr103His
NM_003755.3:c.913T>C NP_003746.2:p.Tyr305His
NM_003755.4:c.913T>C NP_003746.2:p.Tyr305His
NM_003755.5:c.913T>C MANE Select NP_003746.2:p.Tyr305His
Search 100 bp 5'
Search 100 bp 3'