Canonical Allele Identifier: CA346197086

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• ClinVar Variation Id: 1803175
• ClinVar RCV Id: RCV002466845
• gnomAD v4: 2-27364799-T-C
• MyVariant Identifiers: chr2:g.27587666T>C (hg19) ; chr2:g.27364799T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364799T>C , CM000664.2:g.27364799T>C	GRCh38
NC_000002.11:g.27587666T>C , CM000664.1:g.27587666T>C	GRCh37
NC_000002.10:g.27441170T>C	NCBI36
NG_009305.1:g.10659A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1291A>G (EIF2B4) MANE Select	ENSP00000233552.6:p.Asn431Asp
ENST00000347454.8:c.1291A>G (EIF2B4)	ENSP00000233552.5:p.Asn431Asp
ENST00000405940.6:c.*557A>G (EIF2B4)	ENSP00000384375.2:n.*557A>G
ENST00000445933.6:c.1288A>G (EIF2B4)	ENSP00000394397.2:p.Asn430Asp
ENST00000451130.6:c.1351A>G (EIF2B4)	ENSP00000394869.2:p.Asn451Asp
ENST00000478311.1:n.284A>G (EIF2B4)
ENST00000493344.6:c.1354A>G (EIF2B4)	ENSP00000429323.1:p.Asn452Asp
ENST00000616081.4:c.1282A>G (EIF2B4)	ENSP00000477710.1:p.Asn428Asp
ENST00000622434.4:c.*557A>G (EIF2B4)	ENSP00000479991.1:n.*557A>G
NM_001034116.1:c.1291A>G (EIF2B4)	NP_001029288.1:p.Asn431Asp
NM_015636.3:c.1288A>G (EIF2B4)	NP_056451.3:p.Asn430Asp
NM_172195.3:c.1351A>G (EIF2B4)	NP_751945.2:p.Asn451Asp
XM_005264632.1:c.1246A>G (EIF2B4)	XP_005264689.1:p.Asn416Asp
XM_006712132.1:c.1243A>G (EIF2B4)	XP_006712195.1:p.Asn415Asp
XM_011533147.1:c.673A>G (EIF2B4)	XP_011531449.1:p.Asn225Asp
XR_939868.1:n.1772-2625T>C (GTF3C2-AS2)
NM_001318965.1:c.1354A>G (EIF2B4)	NP_001305894.1:p.Asn452Asp
NM_001318966.1:c.1246A>G (EIF2B4)	NP_001305895.1:p.Asn416Asp
NM_001318967.1:c.1198A>G (EIF2B4)	NP_001305896.1:p.Asn400Asp
NM_001318968.1:c.706A>G (EIF2B4)	NP_001305897.1:p.Asn236Asp
NM_001318969.1:c.673A>G (EIF2B4)	NP_001305898.1:p.Asn225Asp
XM_011533147.2:c.673A>G (EIF2B4)	XP_011531449.1:p.Asn225Asp
NM_001034116.2:c.1291A>G (EIF2B4) MANE Select	NP_001029288.1:p.Asn431Asp
NM_001318965.2:c.1354A>G (EIF2B4)	NP_001305894.1:p.Asn452Asp
NM_001318966.2:c.1246A>G (EIF2B4)	NP_001305895.1:p.Asn416Asp
NM_001318967.2:c.1198A>G (EIF2B4)	NP_001305896.1:p.Asn400Asp
NM_001318968.2:c.706A>G (EIF2B4)	NP_001305897.1:p.Asn236Asp
NM_001318969.2:c.673A>G (EIF2B4)	NP_001305898.1:p.Asn225Asp
NM_015636.4:c.1288A>G (EIF2B4)	NP_056451.3:p.Asn430Asp
NM_172195.4:c.1351A>G (EIF2B4)	NP_751945.2:p.Asn451Asp