Canonical Allele Identifier: CA505466770
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226157G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115481G>C , CM000681.2:g.10115481G>C GRCh38
NC_000019.9:g.10226157G>C , CM000681.1:g.10226157G>C GRCh37
NC_000019.8:g.10087157G>C NCBI36
NG_047007.1:g.8961G>C
NG_051197.1:g.9444C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.945C>G MANE Select ENSP00000253108.3:p.Ala315=
ENST00000253108.8:c.945C>G ENSP00000253108.3:p.Ala315=
ENST00000590158.1:n.964C>G
ENST00000593054.5:c.339C>G ENSP00000467187.1:p.Ala113=
NM_003755.3:c.945C>G NP_003746.2:p.Ala315=
NM_003755.4:c.945C>G NP_003746.2:p.Ala315=
NM_003755.5:c.945C>G MANE Select NP_003746.2:p.Ala315=
Search 100 bp 5'
Search 100 bp 3'