Canonical Allele Identifier: CA2726464

Gene: EIF2B5

Linked Data

• dbSNP Id: rs776915774
• ExAC: 3:183855977 T / C
• gnomAD v2: 3-183855977-T-C
• gnomAD v4: 3-184138189-T-C
• MyVariant Identifiers: chr3:g.183855977T>C (hg19) ; chr3:g.184138189T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138189T>C , CM000665.2:g.184138189T>C	GRCh38
NC_000003.11:g.183855977T>C , CM000665.1:g.183855977T>C	GRCh37
NC_000003.10:g.185338671T>C	NCBI36
NG_015826.1:g.8168T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.731T>C
ENST00000468748.7:n.691T>C
ENST00000484154.2:n.1329T>C
ENST00000491008.6:n.1456T>C
ENST00000492226.2:n.705T>C
ENST00000492773.6:c.462T>C
ENST00000647636.1:c.708T>C	ENSP00000497505.1:p.Asp236=
ENST00000647909.1:c.732T>C	ENSP00000498164.1:p.Asp244=
ENST00000648145.1:c.476T>C
ENST00000648189.1:c.458T>C
ENST00000648256.1:c.657T>C	ENSP00000497356.1:p.Asp219=
ENST00000648314.1:c.708T>C	ENSP00000496920.1:p.Asp236=
ENST00000648599.1:c.708T>C	ENSP00000497159.1:p.Asp236=
ENST00000648630.1:c.702T>C	ENSP00000497887.1:p.Asp234=
ENST00000648682.1:c.708T>C	ENSP00000498185.1:p.Asp236=
ENST00000648882.1:c.*534T>C	ENSP00000497603.1:n.*534T>C
ENST00000648890.1:c.708T>C	ENSP00000497503.1:p.Asp236=
ENST00000648915.2:c.708T>C MANE Select	ENSP00000497160.1:p.Asp236=
ENST00000649545.1:c.442T>C
ENST00000649688.1:c.708T>C	ENSP00000497097.1:p.Asp236=
ENST00000649814.1:n.757T>C
ENST00000650270.1:c.575T>C
ENST00000273783.7:c.708T>C	ENSP00000273783.3:p.Asp236=
ENST00000432982.5:c.245+1514T>C
ENST00000444495.1:c.708T>C	ENSP00000409142.1:p.Asp236=
ENST00000468748.5:n.161T>C
ENST00000479833.1:n.24T>C
ENST00000481054.5:n.709T>C
ENST00000491008.5:n.672T>C
ENST00000491144.5:n.1148T>C
NM_003907.2:c.708T>C	NP_003898.2:p.Asp236=
XR_924208.1:n.1659T>C
NM_003907.3:c.708T>C MANE Select	NP_003898.2:p.Asp236=
XM_011513266.3:c.-194T>C	XP_011511568.1:n.-194T>C
XR_001740352.2:n.1071T>C
XR_001740353.2:n.1071T>C
XR_924208.2:n.1071T>C