Canonical Allele Identifier: CA2726438

Gene: EIF2B5

Linked Data

• dbSNP Id: rs773051587
• ExAC: 3:183855844 G / A
• gnomAD v2: 3-183855844-G-A
• gnomAD v4: 3-184138056-G-A
• MyVariant Identifiers: chr3:g.183855844G>A (hg19) ; chr3:g.184138056G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138056G>A , CM000665.2:g.184138056G>A	GRCh38
NC_000003.11:g.183855844G>A , CM000665.1:g.183855844G>A	GRCh37
NC_000003.10:g.185338538G>A	NCBI36
NG_015826.1:g.8035G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.688G>A
ENST00000468748.7:n.648G>A
ENST00000484154.2:n.1286G>A
ENST00000491008.6:n.1413G>A
ENST00000492226.2:n.662G>A
ENST00000492773.6:c.397G>A
ENST00000647636.1:c.665G>A	ENSP00000497505.1:p.Arg222Gln
ENST00000647909.1:c.689G>A	ENSP00000498164.1:p.Arg230Gln
ENST00000648145.1:c.433G>A
ENST00000648189.1:c.415G>A
ENST00000648256.1:c.614G>A	ENSP00000497356.1:p.Arg205Gln
ENST00000648314.1:c.665G>A	ENSP00000496920.1:p.Arg222Gln
ENST00000648599.1:c.665G>A	ENSP00000497159.1:p.Arg222Gln
ENST00000648630.1:c.659G>A	ENSP00000497887.1:p.Arg220Gln
ENST00000648682.1:c.665G>A	ENSP00000498185.1:p.Arg222Gln
ENST00000648882.1:c.*491G>A	ENSP00000497603.1:n.*491G>A
ENST00000648890.1:c.665G>A	ENSP00000497503.1:p.Arg222Gln
ENST00000648915.2:c.665G>A MANE Select	ENSP00000497160.1:p.Arg222Gln
ENST00000649545.1:c.399G>A
ENST00000649688.1:c.665G>A	ENSP00000497097.1:p.Arg222Gln
ENST00000649814.1:n.714G>A
ENST00000650270.1:c.532G>A
ENST00000273783.7:c.665G>A	ENSP00000273783.3:p.Arg222Gln
ENST00000432982.5:c.245+1381G>A
ENST00000444495.1:c.665G>A	ENSP00000409142.1:p.Arg222Gln
ENST00000468748.5:n.118G>A
ENST00000481054.5:n.666G>A
ENST00000491008.5:n.629G>A
ENST00000491144.5:n.1105G>A
NM_003907.2:c.665G>A	NP_003898.2:p.Arg222Gln
XR_924208.1:n.1616G>A
NM_003907.3:c.665G>A MANE Select	NP_003898.2:p.Arg222Gln
XM_011513266.3:c.-237G>A	XP_011511568.1:n.-237G>A
XR_001740352.2:n.1028G>A
XR_001740353.2:n.1028G>A
XR_924208.2:n.1028G>A