Canonical Allele Identifier: CA9186838
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs772956400
ExAC: 19:10226334 CCCA / C
gnomAD v2: 19-10226334-CCCA-C
gnomAD v4: 19-10115658-CCCA-C
MyVariant Identifiers: chr19:g.10226335_10226337del (hg19) chr19:g.10115659_10115661del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115661_10115663del , CM000681.2:g.10115661_10115663del GRCh38
NC_000019.9:g.10226337_10226339del , CM000681.1:g.10226337_10226339del GRCh37
NC_000019.8:g.10087337_10087339del NCBI36
NG_047007.1:g.9141_9143del
NG_051197.1:g.9264_9266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+23_840+25del MANE Select ENSP00000253108.3:n.840+23_840+25del
ENST00000253108.8:c.840+23_840+25del ENSP00000253108.3:n.840+23_840+25del
ENST00000589454.5:c.816+23_816+25del ENSP00000466860.1:n.816+23_816+25del
ENST00000590158.1:n.859+23_859+25del
ENST00000593054.5:c.234+23_234+25del ENSP00000467187.1:n.234+23_234+25del
NM_003755.3:c.840+23_840+25del NP_003746.2:n.840+23_840+25del
NM_003755.4:c.840+23_840+25del NP_003746.2:n.840+23_840+25del
NM_003755.5:c.840+23_840+25del MANE Select NP_003746.2:n.840+23_840+25del
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