Canonical Allele Identifier: CA505466854
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs1467558355
gnomAD v2: 19-10226202-C-G
gnomAD v3: 19-10115526-C-G
gnomAD v4: 19-10115526-C-G
MyVariant Identifiers: chr19:g.10226202C>G (hg19) chr19:g.10115526C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115526C>G , CM000681.2:g.10115526C>G GRCh38
NC_000019.9:g.10226202C>G , CM000681.1:g.10226202C>G GRCh37
NC_000019.8:g.10087202C>G NCBI36
NG_047007.1:g.9006C>G
NG_051197.1:g.9399G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.900G>C MANE Select ENSP00000253108.3:p.Val300=
ENST00000253108.8:c.900G>C ENSP00000253108.3:p.Val300=
ENST00000590158.1:n.919G>C
ENST00000593054.5:c.294G>C ENSP00000467187.1:p.Val98=
NM_003755.3:c.900G>C NP_003746.2:p.Val300=
NM_003755.4:c.900G>C NP_003746.2:p.Val300=
NM_003755.5:c.900G>C MANE Select NP_003746.2:p.Val300=
Search 100 bp 5'
Search 100 bp 3'