Canonical Allele Identifier: CA346196961

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587630A>C (hg19) ; chr2:g.27364763A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364763A>C , CM000664.2:g.27364763A>C	GRCh38
NC_000002.11:g.27587630A>C , CM000664.1:g.27587630A>C	GRCh37
NC_000002.10:g.27441134A>C	NCBI36
NG_009305.1:g.10695T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1327T>G (EIF2B4) MANE Select	ENSP00000233552.6:p.Phe443Val
ENST00000347454.8:c.1327T>G (EIF2B4)	ENSP00000233552.5:p.Phe443Val
ENST00000405940.6:c.*593T>G (EIF2B4)	ENSP00000384375.2:n.*593T>G
ENST00000445933.6:c.1324T>G (EIF2B4)	ENSP00000394397.2:p.Phe442Val
ENST00000451130.6:c.1387T>G (EIF2B4)	ENSP00000394869.2:p.Phe463Val
ENST00000478311.1:n.320T>G (EIF2B4)
ENST00000493344.6:c.1390T>G (EIF2B4)	ENSP00000429323.1:p.Phe464Val
ENST00000616081.4:c.1318T>G (EIF2B4)	ENSP00000477710.1:p.Phe440Val
ENST00000622434.4:c.*593T>G (EIF2B4)	ENSP00000479991.1:n.*593T>G
NM_001034116.1:c.1327T>G (EIF2B4)	NP_001029288.1:p.Phe443Val
NM_015636.3:c.1324T>G (EIF2B4)	NP_056451.3:p.Phe442Val
NM_172195.3:c.1387T>G (EIF2B4)	NP_751945.2:p.Phe463Val
XM_005264632.1:c.1282T>G (EIF2B4)	XP_005264689.1:p.Phe428Val
XM_006712132.1:c.1279T>G (EIF2B4)	XP_006712195.1:p.Phe427Val
XM_011533147.1:c.709T>G (EIF2B4)	XP_011531449.1:p.Phe237Val
XR_939868.1:n.1772-2661A>C (GTF3C2-AS2)
NM_001318965.1:c.1390T>G (EIF2B4)	NP_001305894.1:p.Phe464Val
NM_001318966.1:c.1282T>G (EIF2B4)	NP_001305895.1:p.Phe428Val
NM_001318967.1:c.1234T>G (EIF2B4)	NP_001305896.1:p.Phe412Val
NM_001318968.1:c.742T>G (EIF2B4)	NP_001305897.1:p.Phe248Val
NM_001318969.1:c.709T>G (EIF2B4)	NP_001305898.1:p.Phe237Val
XM_011533147.2:c.709T>G (EIF2B4)	XP_011531449.1:p.Phe237Val
NM_001034116.2:c.1327T>G (EIF2B4) MANE Select	NP_001029288.1:p.Phe443Val
NM_001318965.2:c.1390T>G (EIF2B4)	NP_001305894.1:p.Phe464Val
NM_001318966.2:c.1282T>G (EIF2B4)	NP_001305895.1:p.Phe428Val
NM_001318967.2:c.1234T>G (EIF2B4)	NP_001305896.1:p.Phe412Val
NM_001318968.2:c.742T>G (EIF2B4)	NP_001305897.1:p.Phe248Val
NM_001318969.2:c.709T>G (EIF2B4)	NP_001305898.1:p.Phe237Val
NM_015636.4:c.1324T>G (EIF2B4)	NP_056451.3:p.Phe442Val
NM_172195.4:c.1387T>G (EIF2B4)	NP_751945.2:p.Phe463Val