Canonical Allele Identifier: CA403957738
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226188T>C (hg19) chr19:g.10115512T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115512T>C , CM000681.2:g.10115512T>C GRCh38
NC_000019.9:g.10226188T>C , CM000681.1:g.10226188T>C GRCh37
NC_000019.8:g.10087188T>C NCBI36
NG_047007.1:g.8992T>C
NG_051197.1:g.9413A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.914A>G MANE Select ENSP00000253108.3:p.Tyr305Cys
ENST00000253108.8:c.914A>G ENSP00000253108.3:p.Tyr305Cys
ENST00000590158.1:n.933A>G
ENST00000593054.5:c.308A>G ENSP00000467187.1:p.Tyr103Cys
NM_003755.3:c.914A>G NP_003746.2:p.Tyr305Cys
NM_003755.4:c.914A>G NP_003746.2:p.Tyr305Cys
NM_003755.5:c.914A>G MANE Select NP_003746.2:p.Tyr305Cys
Search 100 bp 5'
Search 100 bp 3'