Canonical Allele Identifier: CA346199884

Gene: EIF2B4

Linked Data

• MyVariant Identifiers: chr2:g.27590682T>C (hg19) ; chr2:g.27367815T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27367815T>C , CM000664.2:g.27367815T>C	GRCh38
NC_000002.11:g.27590682T>C , CM000664.1:g.27590682T>C	GRCh37
NC_000002.10:g.27444186T>C	NCBI36
NG_009305.1:g.7643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.713A>G MANE Select	ENSP00000233552.6:p.Gln238Arg
ENST00000347454.8:c.713A>G	ENSP00000233552.5:p.Gln238Arg
ENST00000405940.6:c.687A>G	ENSP00000384375.2:p.Ser229=
ENST00000417567.1:c.289A>G
ENST00000445933.6:c.710A>G	ENSP00000394397.2:p.Gln237Arg
ENST00000451130.6:c.773A>G	ENSP00000394869.2:p.Gln258Arg
ENST00000475582.5:n.2036A>G
ENST00000493344.6:c.776A>G	ENSP00000429323.1:p.Gln259Arg
ENST00000616081.4:c.704A>G	ENSP00000477710.1:p.Gln235Arg
ENST00000622434.4:c.668A>G	ENSP00000479991.1:p.Gln223Arg
NM_001034116.1:c.713A>G	NP_001029288.1:p.Gln238Arg
NM_015636.3:c.710A>G	NP_056451.3:p.Gln237Arg
NM_172195.3:c.773A>G	NP_751945.2:p.Gln258Arg
XM_005264632.1:c.668A>G	XP_005264689.1:p.Gln223Arg
XM_006712132.1:c.665A>G	XP_006712195.1:p.Gln222Arg
XM_011533147.1:c.95A>G	XP_011531449.1:p.Gln32Arg
NM_001318965.1:c.776A>G	NP_001305894.1:p.Gln259Arg
NM_001318966.1:c.668A>G	NP_001305895.1:p.Gln223Arg
NM_001318967.1:c.620A>G	NP_001305896.1:p.Gln207Arg
NM_001318968.1:c.128A>G	NP_001305897.1:p.Gln43Arg
NM_001318969.1:c.95A>G	NP_001305898.1:p.Gln32Arg
XM_011533147.2:c.95A>G	XP_011531449.1:p.Gln32Arg
NM_001034116.2:c.713A>G MANE Select	NP_001029288.1:p.Gln238Arg
NM_001318965.2:c.776A>G	NP_001305894.1:p.Gln259Arg
NM_001318966.2:c.668A>G	NP_001305895.1:p.Gln223Arg
NM_001318967.2:c.620A>G	NP_001305896.1:p.Gln207Arg
NM_001318968.2:c.128A>G	NP_001305897.1:p.Gln43Arg
NM_001318969.2:c.95A>G	NP_001305898.1:p.Gln32Arg
NM_015636.4:c.710A>G	NP_056451.3:p.Gln237Arg
NM_172195.4:c.773A>G	NP_751945.2:p.Gln258Arg