Canonical Allele Identifier: CA346197902

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27589702G>C (hg19) ; chr2:g.27366835G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27366835G>C , CM000664.2:g.27366835G>C	GRCh38
NC_000002.11:g.27589702G>C , CM000664.1:g.27589702G>C	GRCh37
NC_000002.10:g.27443206G>C	NCBI36
NG_009305.1:g.8623C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1115C>G (EIF2B4) MANE Select	ENSP00000233552.6:p.Thr372Arg
ENST00000347454.8:c.1115C>G (EIF2B4)	ENSP00000233552.5:p.Thr372Arg
ENST00000405940.6:c.*381C>G (EIF2B4)	ENSP00000384375.2:n.*381C>G
ENST00000417567.1:c.689C>G (EIF2B4)
ENST00000445933.6:c.1112C>G (EIF2B4)	ENSP00000394397.2:p.Thr371Arg
ENST00000451130.6:c.1175C>G (EIF2B4)	ENSP00000394869.2:p.Thr392Arg
ENST00000475582.5:n.3016C>G (EIF2B4)
ENST00000493344.6:c.1178C>G (EIF2B4)	ENSP00000429323.1:p.Thr393Arg
ENST00000616081.4:c.1106C>G (EIF2B4)	ENSP00000477710.1:p.Thr369Arg
ENST00000622434.4:c.*381C>G (EIF2B4)	ENSP00000479991.1:n.*381C>G
NM_001034116.1:c.1115C>G (EIF2B4)	NP_001029288.1:p.Thr372Arg
NM_015636.3:c.1112C>G (EIF2B4)	NP_056451.3:p.Thr371Arg
NM_172195.3:c.1175C>G (EIF2B4)	NP_751945.2:p.Thr392Arg
XM_005264632.1:c.1070C>G (EIF2B4)	XP_005264689.1:p.Thr357Arg
XM_006712132.1:c.1067C>G (EIF2B4)	XP_006712195.1:p.Thr356Arg
XM_011533147.1:c.497C>G (EIF2B4)	XP_011531449.1:p.Thr166Arg
XR_939868.1:n.1772-589G>C (GTF3C2-AS2)
NM_001318965.1:c.1178C>G (EIF2B4)	NP_001305894.1:p.Thr393Arg
NM_001318966.1:c.1070C>G (EIF2B4)	NP_001305895.1:p.Thr357Arg
NM_001318967.1:c.1022C>G (EIF2B4)	NP_001305896.1:p.Thr341Arg
NM_001318968.1:c.530C>G (EIF2B4)	NP_001305897.1:p.Thr177Arg
NM_001318969.1:c.497C>G (EIF2B4)	NP_001305898.1:p.Thr166Arg
XM_011533147.2:c.497C>G (EIF2B4)	XP_011531449.1:p.Thr166Arg
NM_001034116.2:c.1115C>G (EIF2B4) MANE Select	NP_001029288.1:p.Thr372Arg
NM_001318965.2:c.1178C>G (EIF2B4)	NP_001305894.1:p.Thr393Arg
NM_001318966.2:c.1070C>G (EIF2B4)	NP_001305895.1:p.Thr357Arg
NM_001318967.2:c.1022C>G (EIF2B4)	NP_001305896.1:p.Thr341Arg
NM_001318968.2:c.530C>G (EIF2B4)	NP_001305897.1:p.Thr177Arg
NM_001318969.2:c.497C>G (EIF2B4)	NP_001305898.1:p.Thr166Arg
NM_015636.4:c.1112C>G (EIF2B4)	NP_056451.3:p.Thr371Arg
NM_172195.4:c.1175C>G (EIF2B4)	NP_751945.2:p.Thr392Arg