Canonical Allele Identifier: CA347591409

Gene: EIF2AK3

Linked Data

• dbSNP Id: rs1674419775
• MyVariant Identifiers: chr2:g.88874567C>G (hg19) ; chr2:g.88575049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575049C>G , CM000664.2:g.88575049C>G	GRCh38
NC_000002.11:g.88874567C>G , CM000664.1:g.88874567C>G	GRCh37
NC_000002.10:g.88655682C>G	NCBI36
NG_016424.1:g.57528G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2262G>C
ENST00000682276.1:n.1879G>C
ENST00000682892.1:c.1981G>C	ENSP00000507214.1:p.Gly661Arg
ENST00000682952.1:n.2073G>C
ENST00000684455.1:c.1647G>C
ENST00000684642.1:c.1831G>C	ENSP00000507355.1:p.Gly611Arg
ENST00000684740.1:n.2612G>C
ENST00000303236.9:c.2434G>C MANE Select	ENSP00000307235.3:p.Gly812Arg
ENST00000652099.1:c.2628G>C
ENST00000652736.1:n.2310G>C
ENST00000303236.7:c.2434G>C	ENSP00000307235.3:p.Gly812Arg
ENST00000415570.1:c.2071G>C	ENSP00000412076.1:p.Gly691Arg
ENST00000419748.5:c.1981G>C	ENSP00000408325.1:p.Gly661Arg
ENST00000470706.1:n.77G>C
NM_001313915.1:c.1981G>C	NP_001300844.1:p.Gly661Arg
NM_004836.5:c.2434G>C	NP_004827.4:p.Gly812Arg
NM_004836.6:c.2434G>C	NP_004827.4:p.Gly812Arg
NR_110236.1:n.1186C>G
XM_005264649.3:c.1750G>C	XP_005264706.1:p.Gly584Arg
XM_017005376.2:c.1750G>C	XP_016860865.1:p.Gly584Arg
NM_004836.7:c.2434G>C MANE Select	NP_004827.4:p.Gly812Arg
NM_001313915.2:c.1981G>C	NP_001300844.1:p.Gly661Arg