Canonical Allele Identifier: CA403957704
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1599324606
MyVariant Identifiers: chr19:g.10226182T>G (hg19) chr19:g.10115506T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115506T>G , CM000681.2:g.10115506T>G GRCh38
NC_000019.9:g.10226182T>G , CM000681.1:g.10226182T>G GRCh37
NC_000019.8:g.10087182T>G NCBI36
NG_047007.1:g.8986T>G
NG_051197.1:g.9419A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.920A>C MANE Select ENSP00000253108.3:p.His307Pro
ENST00000253108.8:c.920A>C ENSP00000253108.3:p.His307Pro
ENST00000590158.1:n.939A>C
ENST00000593054.5:c.314A>C ENSP00000467187.1:p.His105Pro
NM_003755.3:c.920A>C NP_003746.2:p.His307Pro
NM_003755.4:c.920A>C NP_003746.2:p.His307Pro
NM_003755.5:c.920A>C MANE Select NP_003746.2:p.His307Pro
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