Canonical Allele Identifier: CA355382422

Gene: EIF2B5

Linked Data

• dbSNP Id: rs2109007207
• MyVariant Identifiers: chr3:g.183855826A>G (hg19) ; chr3:g.184138038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138038A>G , CM000665.2:g.184138038A>G	GRCh38
NC_000003.11:g.183855826A>G , CM000665.1:g.183855826A>G	GRCh37
NC_000003.10:g.185338520A>G	NCBI36
NG_015826.1:g.8017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.670A>G
ENST00000468748.7:n.630A>G
ENST00000484154.2:n.1268A>G
ENST00000491008.6:n.1395A>G
ENST00000492226.2:n.644A>G
ENST00000492773.6:c.379A>G
ENST00000647636.1:c.647A>G	ENSP00000497505.1:p.Gln216Arg
ENST00000647909.1:c.671A>G	ENSP00000498164.1:p.Gln224Arg
ENST00000648145.1:c.415A>G
ENST00000648189.1:c.397A>G
ENST00000648256.1:c.596A>G	ENSP00000497356.1:p.Gln199Arg
ENST00000648314.1:c.647A>G	ENSP00000496920.1:p.Gln216Arg
ENST00000648599.1:c.647A>G	ENSP00000497159.1:p.Gln216Arg
ENST00000648630.1:c.641A>G	ENSP00000497887.1:p.Gln214Arg
ENST00000648682.1:c.647A>G	ENSP00000498185.1:p.Gln216Arg
ENST00000648882.1:c.*473A>G	ENSP00000497603.1:n.*473A>G
ENST00000648890.1:c.647A>G	ENSP00000497503.1:p.Gln216Arg
ENST00000648915.2:c.647A>G MANE Select	ENSP00000497160.1:p.Gln216Arg
ENST00000649545.1:c.381A>G
ENST00000649688.1:c.647A>G	ENSP00000497097.1:p.Gln216Arg
ENST00000649814.1:n.696A>G
ENST00000650270.1:c.514A>G
ENST00000273783.7:c.647A>G	ENSP00000273783.3:p.Gln216Arg
ENST00000432982.5:c.245+1363A>G
ENST00000444495.1:c.647A>G	ENSP00000409142.1:p.Gln216Arg
ENST00000468748.5:n.100A>G
ENST00000481054.5:n.648A>G
ENST00000491008.5:n.611A>G
ENST00000491144.5:n.1087A>G
NM_003907.2:c.647A>G	NP_003898.2:p.Gln216Arg
XR_924208.1:n.1598A>G
NM_003907.3:c.647A>G MANE Select	NP_003898.2:p.Gln216Arg
XM_011513266.3:c.-255A>G	XP_011511568.1:n.-255A>G
XR_001740352.2:n.1010A>G
XR_001740353.2:n.1010A>G
XR_924208.2:n.1010A>G