Canonical Allele Identifier: CA783165952

Gene: EIF3G

Linked Data

• dbSNP Id: rs1406155376
• gnomAD v3: 19-10115592-A-G
• gnomAD v4: 19-10115592-A-G
• MyVariant Identifiers: chr19:g.10226268A>G (hg19) ; chr19:g.10115592A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115592A>G , CM000681.2:g.10115592A>G	GRCh38
NC_000019.9:g.10226268A>G , CM000681.1:g.10226268A>G	GRCh37
NC_000019.8:g.10087268A>G	NCBI36
NG_047007.1:g.9072A>G
NG_051197.1:g.9333T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.841-7T>C MANE Select	ENSP00000253108.3:n.841-7T>C
ENST00000253108.8:c.841-7T>C	ENSP00000253108.3:n.841-7T>C
ENST00000589454.5:c.817-7T>C	ENSP00000466860.1:n.817-7T>C
ENST00000590158.1:n.860-7T>C
ENST00000593054.5:c.235-7T>C	ENSP00000467187.1:n.235-7T>C
NM_003755.3:c.841-7T>C	NP_003746.2:n.841-7T>C
NM_003755.4:c.841-7T>C	NP_003746.2:n.841-7T>C
NM_003755.5:c.841-7T>C MANE Select	NP_003746.2:n.841-7T>C