Canonical Allele Identifier: CA355382840

Gene: EIF2B5

Linked Data

• dbSNP Id: rs1261473481
• MyVariant Identifiers: chr3:g.183855961T>G (hg19) ; chr3:g.184138173T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138173T>G , CM000665.2:g.184138173T>G	GRCh38
NC_000003.11:g.183855961T>G , CM000665.1:g.183855961T>G	GRCh37
NC_000003.10:g.185338655T>G	NCBI36
NG_015826.1:g.8152T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.715T>G
ENST00000468748.7:n.675T>G
ENST00000484154.2:n.1313T>G
ENST00000491008.6:n.1440T>G
ENST00000492226.2:n.689T>G
ENST00000492773.6:c.446T>G
ENST00000647636.1:c.692T>G	ENSP00000497505.1:p.Phe231Cys
ENST00000647909.1:c.716T>G	ENSP00000498164.1:p.Phe239Cys
ENST00000648145.1:c.460T>G
ENST00000648189.1:c.442T>G
ENST00000648256.1:c.641T>G	ENSP00000497356.1:p.Phe214Cys
ENST00000648314.1:c.692T>G	ENSP00000496920.1:p.Phe231Cys
ENST00000648599.1:c.692T>G	ENSP00000497159.1:p.Phe231Cys
ENST00000648630.1:c.686T>G	ENSP00000497887.1:p.Phe229Cys
ENST00000648682.1:c.692T>G	ENSP00000498185.1:p.Phe231Cys
ENST00000648882.1:c.*518T>G	ENSP00000497603.1:n.*518T>G
ENST00000648890.1:c.692T>G	ENSP00000497503.1:p.Phe231Cys
ENST00000648915.2:c.692T>G MANE Select	ENSP00000497160.1:p.Phe231Cys
ENST00000649545.1:c.426T>G
ENST00000649688.1:c.692T>G	ENSP00000497097.1:p.Phe231Cys
ENST00000649814.1:n.741T>G
ENST00000650270.1:c.559T>G
ENST00000273783.7:c.692T>G	ENSP00000273783.3:p.Phe231Cys
ENST00000432982.5:c.245+1498T>G
ENST00000444495.1:c.692T>G	ENSP00000409142.1:p.Phe231Cys
ENST00000468748.5:n.145T>G
ENST00000479833.1:n.8T>G
ENST00000481054.5:n.693T>G
ENST00000491008.5:n.656T>G
ENST00000491144.5:n.1132T>G
NM_003907.2:c.692T>G	NP_003898.2:p.Phe231Cys
XR_924208.1:n.1643T>G
NM_003907.3:c.692T>G MANE Select	NP_003898.2:p.Phe231Cys
XM_011513266.3:c.-210T>G	XP_011511568.1:n.-210T>G
XR_001740352.2:n.1055T>G
XR_001740353.2:n.1055T>G
XR_924208.2:n.1055T>G