Canonical Allele Identifier: CA548394818
Gene: EIF2B5 HGNC NCBI

Linked Data

dbSNP Id: rs1238676631

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137569A>G , CM000665.2:g.184137569A>G GRCh38
NC_000003.11:g.183855357A>G , CM000665.1:g.183855357A>G GRCh37
NC_000003.10:g.185338051A>G NCBI36
NG_015826.1:g.7548A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.344-51A>G
ENST00000468748.7:n.304-51A>G
ENST00000484154.2:n.891A>G
ENST00000491008.6:n.1018A>G
ENST00000492226.2:n.318-51A>G
ENST00000492773.6:c.53-51A>G
ENST00000647636.1:c.321-51A>G ENSP00000497505.1:n.321-51A>G
ENST00000647909.1:c.321-51A>G ENSP00000498164.1:n.321-51A>G
ENST00000648145.1:c.89-51A>G
ENST00000648189.1:c.71-51A>G
ENST00000648256.1:c.270-51A>G ENSP00000497356.1:n.270-51A>G
ENST00000648314.1:c.321-51A>G ENSP00000496920.1:n.321-51A>G
ENST00000648599.1:c.321-51A>G ENSP00000497159.1:n.321-51A>G
ENST00000648630.1:c.315-51A>G ENSP00000497887.1:n.315-51A>G
ENST00000648682.1:c.321-51A>G ENSP00000498185.1:n.321-51A>G
ENST00000648882.1:c.*147-51A>G ENSP00000497603.1:n.*147-51A>G
ENST00000648890.1:c.321-51A>G ENSP00000497503.1:n.321-51A>G
ENST00000648915.2:c.321-51A>G MANE Select ENSP00000497160.1:n.321-51A>G
ENST00000649545.1:c.55-51A>G
ENST00000649688.1:c.321-51A>G ENSP00000497097.1:n.321-51A>G
ENST00000649814.1:n.370-51A>G
ENST00000650244.1:c.466-51A>G ENSP00000497227.1:n.466-51A>G
ENST00000650270.1:c.188-51A>G
ENST00000273783.7:c.321-51A>G ENSP00000273783.3:n.321-51A>G
ENST00000432982.5:c.245+894A>G
ENST00000444495.1:c.321-51A>G ENSP00000409142.1:n.321-51A>G
ENST00000481054.5:n.322-51A>G
ENST00000491008.5:n.234A>G
ENST00000491144.5:n.669-51A>G
ENST00000498831.1:n.275+39A>G
NM_003907.2:c.321-51A>G NP_003898.2:n.321-51A>G
XR_924208.1:n.1272-51A>G
NM_003907.3:c.321-51A>G MANE Select NP_003898.2:n.321-51A>G
XM_011513266.3:c.-581-51A>G XP_011511568.1:n.-581-51A>G
XR_001740352.2:n.684-51A>G
XR_001740353.2:n.684-51A>G
XR_924208.2:n.684-51A>G