Canonical Allele Identifier: CA437323597

Gene: EIF2B5

Linked Data

• dbSNP Id: rs1338200222
• gnomAD v2: 3-183855791-T-C
• gnomAD v3: 3-184138003-T-C
• gnomAD v4: 3-184138003-T-C
• MyVariant Identifiers: chr3:g.183855791T>C (hg19) ; chr3:g.184138003T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138003T>C , CM000665.2:g.184138003T>C	GRCh38
NC_000003.11:g.183855791T>C , CM000665.1:g.183855791T>C	GRCh37
NC_000003.10:g.185338485T>C	NCBI36
NG_015826.1:g.7982T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.635T>C
ENST00000468748.7:n.595T>C
ENST00000484154.2:n.1233T>C
ENST00000491008.6:n.1360T>C
ENST00000492226.2:n.609T>C
ENST00000492773.6:c.344T>C
ENST00000647636.1:c.612T>C	ENSP00000497505.1:p.Ala204=
ENST00000647909.1:c.636T>C	ENSP00000498164.1:p.Ala212=
ENST00000648145.1:c.380T>C
ENST00000648189.1:c.362T>C
ENST00000648256.1:c.561T>C	ENSP00000497356.1:p.Ala187=
ENST00000648314.1:c.612T>C	ENSP00000496920.1:p.Ala204=
ENST00000648599.1:c.612T>C	ENSP00000497159.1:p.Ala204=
ENST00000648630.1:c.606T>C	ENSP00000497887.1:p.Ala202=
ENST00000648682.1:c.612T>C	ENSP00000498185.1:p.Ala204=
ENST00000648882.1:c.*438T>C	ENSP00000497603.1:n.*438T>C
ENST00000648890.1:c.612T>C	ENSP00000497503.1:p.Ala204=
ENST00000648915.2:c.612T>C MANE Select	ENSP00000497160.1:p.Ala204=
ENST00000649545.1:c.346T>C
ENST00000649688.1:c.612T>C	ENSP00000497097.1:p.Ala204=
ENST00000649814.1:n.661T>C
ENST00000650270.1:c.479T>C
ENST00000273783.7:c.612T>C	ENSP00000273783.3:p.Ala204=
ENST00000432982.5:c.245+1328T>C
ENST00000444495.1:c.612T>C	ENSP00000409142.1:p.Ala204=
ENST00000468748.5:n.65T>C
ENST00000481054.5:n.613T>C
ENST00000491008.5:n.576T>C
ENST00000491144.5:n.1052T>C
ENST00000498831.1:n.567T>C
NM_003907.2:c.612T>C	NP_003898.2:p.Ala204=
XR_924208.1:n.1563T>C
NM_003907.3:c.612T>C MANE Select	NP_003898.2:p.Ala204=
XM_011513266.3:c.-290T>C	XP_011511568.1:n.-290T>C
XR_001740352.2:n.975T>C
XR_001740353.2:n.975T>C
XR_924208.2:n.975T>C