Canonical Allele Identifier: CA505466846
Gene: EIF3G HGNC NCBI

Linked Data

gnomAD v4: 19-10115523-G-C
MyVariant Identifiers: chr19:g.10226199G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115523G>C , CM000681.2:g.10115523G>C GRCh38
NC_000019.9:g.10226199G>C , CM000681.1:g.10226199G>C GRCh37
NC_000019.8:g.10087199G>C NCBI36
NG_047007.1:g.9003G>C
NG_051197.1:g.9402C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.903C>G MANE Select ENSP00000253108.3:p.Ser301=
ENST00000253108.8:c.903C>G ENSP00000253108.3:p.Ser301=
ENST00000590158.1:n.922C>G
ENST00000593054.5:c.297C>G ENSP00000467187.1:p.Ser99=
NM_003755.3:c.903C>G NP_003746.2:p.Ser301=
NM_003755.4:c.903C>G NP_003746.2:p.Ser301=
NM_003755.5:c.903C>G MANE Select NP_003746.2:p.Ser301=
Search 100 bp 5'
Search 100 bp 3'