Canonical Allele Identifier: CA355382406

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184138032-A-G
• MyVariant Identifiers: chr3:g.183855820A>G (hg19) ; chr3:g.184138032A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138032A>G , CM000665.2:g.184138032A>G	GRCh38
NC_000003.11:g.183855820A>G , CM000665.1:g.183855820A>G	GRCh37
NC_000003.10:g.185338514A>G	NCBI36
NG_015826.1:g.8011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.664A>G
ENST00000468748.7:n.624A>G
ENST00000484154.2:n.1262A>G
ENST00000491008.6:n.1389A>G
ENST00000492226.2:n.638A>G
ENST00000492773.6:c.373A>G
ENST00000647636.1:c.641A>G	ENSP00000497505.1:p.His214Arg
ENST00000647909.1:c.665A>G	ENSP00000498164.1:p.His222Arg
ENST00000648145.1:c.409A>G
ENST00000648189.1:c.391A>G
ENST00000648256.1:c.590A>G	ENSP00000497356.1:p.His197Arg
ENST00000648314.1:c.641A>G	ENSP00000496920.1:p.His214Arg
ENST00000648599.1:c.641A>G	ENSP00000497159.1:p.His214Arg
ENST00000648630.1:c.635A>G	ENSP00000497887.1:p.His212Arg
ENST00000648682.1:c.641A>G	ENSP00000498185.1:p.His214Arg
ENST00000648882.1:c.*467A>G	ENSP00000497603.1:n.*467A>G
ENST00000648890.1:c.641A>G	ENSP00000497503.1:p.His214Arg
ENST00000648915.2:c.641A>G MANE Select	ENSP00000497160.1:p.His214Arg
ENST00000649545.1:c.375A>G
ENST00000649688.1:c.641A>G	ENSP00000497097.1:p.His214Arg
ENST00000649814.1:n.690A>G
ENST00000650270.1:c.508A>G
ENST00000273783.7:c.641A>G	ENSP00000273783.3:p.His214Arg
ENST00000432982.5:c.245+1357A>G
ENST00000444495.1:c.641A>G	ENSP00000409142.1:p.His214Arg
ENST00000468748.5:n.94A>G
ENST00000481054.5:n.642A>G
ENST00000491008.5:n.605A>G
ENST00000491144.5:n.1081A>G
ENST00000498831.1:n.596A>G
NM_003907.2:c.641A>G	NP_003898.2:p.His214Arg
XR_924208.1:n.1592A>G
NM_003907.3:c.641A>G MANE Select	NP_003898.2:p.His214Arg
XM_011513266.3:c.-261A>G	XP_011511568.1:n.-261A>G
XR_001740352.2:n.1004A>G
XR_001740353.2:n.1004A>G
XR_924208.2:n.1004A>G