Canonical Allele Identifier: CA425606618

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27589704G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27366837G>A , CM000664.2:g.27366837G>A	GRCh38
NC_000002.11:g.27589704G>A , CM000664.1:g.27589704G>A	GRCh37
NC_000002.10:g.27443208G>A	NCBI36
NG_009305.1:g.8621C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1113C>T (EIF2B4) MANE Select	ENSP00000233552.6:p.His371=
ENST00000347454.8:c.1113C>T (EIF2B4)	ENSP00000233552.5:p.His371=
ENST00000405940.6:c.*379C>T (EIF2B4)	ENSP00000384375.2:n.*379C>T
ENST00000417567.1:c.687C>T (EIF2B4)
ENST00000445933.6:c.1110C>T (EIF2B4)	ENSP00000394397.2:p.His370=
ENST00000451130.6:c.1173C>T (EIF2B4)	ENSP00000394869.2:p.His391=
ENST00000475582.5:n.3014C>T (EIF2B4)
ENST00000493344.6:c.1176C>T (EIF2B4)	ENSP00000429323.1:p.His392=
ENST00000616081.4:c.1104C>T (EIF2B4)	ENSP00000477710.1:p.His368=
ENST00000622434.4:c.*379C>T (EIF2B4)	ENSP00000479991.1:n.*379C>T
NM_001034116.1:c.1113C>T (EIF2B4)	NP_001029288.1:p.His371=
NM_015636.3:c.1110C>T (EIF2B4)	NP_056451.3:p.His370=
NM_172195.3:c.1173C>T (EIF2B4)	NP_751945.2:p.His391=
XM_005264632.1:c.1068C>T (EIF2B4)	XP_005264689.1:p.His356=
XM_006712132.1:c.1065C>T (EIF2B4)	XP_006712195.1:p.His355=
XM_011533147.1:c.495C>T (EIF2B4)	XP_011531449.1:p.His165=
XR_939868.1:n.1772-587G>A (GTF3C2-AS2)
NM_001318965.1:c.1176C>T (EIF2B4)	NP_001305894.1:p.His392=
NM_001318966.1:c.1068C>T (EIF2B4)	NP_001305895.1:p.His356=
NM_001318967.1:c.1020C>T (EIF2B4)	NP_001305896.1:p.His340=
NM_001318968.1:c.528C>T (EIF2B4)	NP_001305897.1:p.His176=
NM_001318969.1:c.495C>T (EIF2B4)	NP_001305898.1:p.His165=
XM_011533147.2:c.495C>T (EIF2B4)	XP_011531449.1:p.His165=
NM_001034116.2:c.1113C>T (EIF2B4) MANE Select	NP_001029288.1:p.His371=
NM_001318965.2:c.1176C>T (EIF2B4)	NP_001305894.1:p.His392=
NM_001318966.2:c.1068C>T (EIF2B4)	NP_001305895.1:p.His356=
NM_001318967.2:c.1020C>T (EIF2B4)	NP_001305896.1:p.His340=
NM_001318968.2:c.528C>T (EIF2B4)	NP_001305897.1:p.His176=
NM_001318969.2:c.495C>T (EIF2B4)	NP_001305898.1:p.His165=
NM_015636.4:c.1110C>T (EIF2B4)	NP_056451.3:p.His370=
NM_172195.4:c.1173C>T (EIF2B4)	NP_751945.2:p.His391=