Canonical Allele Identifier: CA346197310

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• gnomAD v4: 2-27364874-G-A
• COSMIC: COSM4093554 ; COSM4093555
• MyVariant Identifiers: chr2:g.27587741G>A (hg19) ; chr2:g.27364874G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364874G>A , CM000664.2:g.27364874G>A	GRCh38
NC_000002.11:g.27587741G>A , CM000664.1:g.27587741G>A	GRCh37
NC_000002.10:g.27441245G>A	NCBI36
NG_009305.1:g.10584C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1216C>T (EIF2B4) MANE Select	ENSP00000233552.6:p.His406Tyr
ENST00000347454.8:c.1216C>T (EIF2B4)	ENSP00000233552.5:p.His406Tyr
ENST00000405940.6:c.*482C>T (EIF2B4)	ENSP00000384375.2:n.*482C>T
ENST00000445933.6:c.1213C>T (EIF2B4)	ENSP00000394397.2:p.His405Tyr
ENST00000451130.6:c.1276C>T (EIF2B4)	ENSP00000394869.2:p.His426Tyr
ENST00000478311.1:n.209C>T (EIF2B4)
ENST00000493344.6:c.1279C>T (EIF2B4)	ENSP00000429323.1:p.His427Tyr
ENST00000616081.4:c.1207C>T (EIF2B4)	ENSP00000477710.1:p.His403Tyr
ENST00000622434.4:c.*482C>T (EIF2B4)	ENSP00000479991.1:n.*482C>T
NM_001034116.1:c.1216C>T (EIF2B4)	NP_001029288.1:p.His406Tyr
NM_015636.3:c.1213C>T (EIF2B4)	NP_056451.3:p.His405Tyr
NM_172195.3:c.1276C>T (EIF2B4)	NP_751945.2:p.His426Tyr
XM_005264632.1:c.1171C>T (EIF2B4)	XP_005264689.1:p.His391Tyr
XM_006712132.1:c.1168C>T (EIF2B4)	XP_006712195.1:p.His390Tyr
XM_011533147.1:c.598C>T (EIF2B4)	XP_011531449.1:p.His200Tyr
XR_939868.1:n.1772-2550G>A (GTF3C2-AS2)
NM_001318965.1:c.1279C>T (EIF2B4)	NP_001305894.1:p.His427Tyr
NM_001318966.1:c.1171C>T (EIF2B4)	NP_001305895.1:p.His391Tyr
NM_001318967.1:c.1123C>T (EIF2B4)	NP_001305896.1:p.His375Tyr
NM_001318968.1:c.631C>T (EIF2B4)	NP_001305897.1:p.His211Tyr
NM_001318969.1:c.598C>T (EIF2B4)	NP_001305898.1:p.His200Tyr
XM_011533147.2:c.598C>T (EIF2B4)	XP_011531449.1:p.His200Tyr
NM_001034116.2:c.1216C>T (EIF2B4) MANE Select	NP_001029288.1:p.His406Tyr
NM_001318965.2:c.1279C>T (EIF2B4)	NP_001305894.1:p.His427Tyr
NM_001318966.2:c.1171C>T (EIF2B4)	NP_001305895.1:p.His391Tyr
NM_001318967.2:c.1123C>T (EIF2B4)	NP_001305896.1:p.His375Tyr
NM_001318968.2:c.631C>T (EIF2B4)	NP_001305897.1:p.His211Tyr
NM_001318969.2:c.598C>T (EIF2B4)	NP_001305898.1:p.His200Tyr
NM_015636.4:c.1213C>T (EIF2B4)	NP_056451.3:p.His405Tyr
NM_172195.4:c.1276C>T (EIF2B4)	NP_751945.2:p.His426Tyr