Canonical Allele Identifier: CA403957618
Gene: EIF3G HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10226161C>G (hg19) chr19:g.10115485C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115485C>G , CM000681.2:g.10115485C>G GRCh38
NC_000019.9:g.10226161C>G , CM000681.1:g.10226161C>G GRCh37
NC_000019.8:g.10087161C>G NCBI36
NG_047007.1:g.8965C>G
NG_051197.1:g.9440G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.941G>C MANE Select ENSP00000253108.3:p.Trp314Ser
ENST00000253108.8:c.941G>C ENSP00000253108.3:p.Trp314Ser
ENST00000590158.1:n.960G>C
ENST00000593054.5:c.335G>C ENSP00000467187.1:p.Trp112Ser
NM_003755.3:c.941G>C NP_003746.2:p.Trp314Ser
NM_003755.4:c.941G>C NP_003746.2:p.Trp314Ser
NM_003755.5:c.941G>C MANE Select NP_003746.2:p.Trp314Ser
Search 100 bp 5'
Search 100 bp 3'