Canonical Allele Identifier: CA2726300

Gene: EIF2B5

Linked Data

• dbSNP Id: rs755322613
• ExAC: 3:183853181 C / T
• gnomAD v2: 3-183853181-C-T
• MyVariant Identifiers: chr3:g.183853181C>T (hg19) ; chr3:g.184135393C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184135393C>T , CM000665.2:g.184135393C>T	GRCh38
NC_000003.11:g.183853181C>T , CM000665.1:g.183853181C>T	GRCh37
NC_000003.10:g.185335875C>T	NCBI36
NG_015826.1:g.5372C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.8C>T	ENSP00000414775.1:p.Ala3Val
ENST00000465218.3:n.31C>T
ENST00000471832.2:c.8C>T	ENSP00000497786.1:p.Ala3Val
ENST00000492226.2:n.5C>T
ENST00000647636.1:c.8C>T	ENSP00000497505.1:p.Ala3Val
ENST00000647909.1:c.8C>T	ENSP00000498164.1:p.Ala3Val
ENST00000648314.1:c.8C>T	ENSP00000496920.1:p.Ala3Val
ENST00000648599.1:c.8C>T	ENSP00000497159.1:p.Ala3Val
ENST00000648630.1:c.2C>T	ENSP00000497887.1:p.Ala1Val
ENST00000648682.1:c.8C>T	ENSP00000498185.1:p.Ala3Val
ENST00000648882.1:c.8C>T	ENSP00000497603.1:p.Ala3Val
ENST00000648890.1:c.8C>T	ENSP00000497503.1:p.Ala3Val
ENST00000648915.2:c.8C>T MANE Select	ENSP00000497160.1:p.Ala3Val
ENST00000649688.1:c.8C>T	ENSP00000497097.1:p.Ala3Val
ENST00000649814.1:n.57C>T
ENST00000273783.7:c.8C>T	ENSP00000273783.3:p.Ala3Val
ENST00000432569.1:c.8C>T	ENSP00000414775.1:p.Ala3Val
ENST00000444495.1:c.8C>T	ENSP00000409142.1:p.Ala3Val
ENST00000481054.5:n.9C>T
ENST00000491144.5:n.356C>T
NM_003907.2:c.8C>T	NP_003898.2:p.Ala3Val
XR_924208.1:n.959C>T
NM_003907.3:c.8C>T MANE Select	NP_003898.2:p.Ala3Val
XM_011513266.3:c.-894C>T	XP_011511568.1:n.-894C>T
XR_001740352.2:n.371C>T
XR_001740353.2:n.371C>T
XR_924208.2:n.371C>T