Canonical Allele Identifier: CA437145194

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184135433-T-C
• MyVariant Identifiers: chr3:g.183853221T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184135433T>C , CM000665.2:g.184135433T>C	GRCh38
NC_000003.11:g.183853221T>C , CM000665.1:g.183853221T>C	GRCh37
NC_000003.10:g.185335915T>C	NCBI36
NG_015826.1:g.5412T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.48T>C	ENSP00000414775.1:p.Ala16=
ENST00000465218.3:n.71T>C
ENST00000468748.7:n.31T>C
ENST00000471832.2:c.48T>C	ENSP00000497786.1:p.Ala16=
ENST00000492226.2:n.45T>C
ENST00000647636.1:c.48T>C	ENSP00000497505.1:p.Ala16=
ENST00000647909.1:c.48T>C	ENSP00000498164.1:p.Ala16=
ENST00000648314.1:c.48T>C	ENSP00000496920.1:p.Ala16=
ENST00000648599.1:c.48T>C	ENSP00000497159.1:p.Ala16=
ENST00000648630.1:c.42T>C	ENSP00000497887.1:p.Ala14=
ENST00000648682.1:c.48T>C	ENSP00000498185.1:p.Ala16=
ENST00000648882.1:c.48T>C	ENSP00000497603.1:p.Ala16=
ENST00000648890.1:c.48T>C	ENSP00000497503.1:p.Ala16=
ENST00000648915.2:c.48T>C MANE Select	ENSP00000497160.1:p.Ala16=
ENST00000649688.1:c.48T>C	ENSP00000497097.1:p.Ala16=
ENST00000649814.1:n.97T>C
ENST00000273783.7:c.48T>C	ENSP00000273783.3:p.Ala16=
ENST00000432569.1:c.48T>C	ENSP00000414775.1:p.Ala16=
ENST00000432982.5:c.34T>C
ENST00000444495.1:c.48T>C	ENSP00000409142.1:p.Ala16=
ENST00000481054.5:n.49T>C
ENST00000491144.5:n.396T>C
NM_003907.2:c.48T>C	NP_003898.2:p.Ala16=
XR_924208.1:n.999T>C
NM_003907.3:c.48T>C MANE Select	NP_003898.2:p.Ala16=
XM_011513266.3:c.-854T>C	XP_011511568.1:n.-854T>C
XR_001740352.2:n.411T>C
XR_001740353.2:n.411T>C
XR_924208.2:n.411T>C