Canonical Allele Identifier: CA425410167

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• ClinVar Variation Id: 2869618
• ClinVar RCV Id: RCV003700728
• dbSNP Id: rs1681720216
• gnomAD v3: 2-27364785-C-T
• gnomAD v4: 2-27364785-C-T
• MyVariant Identifiers: chr2:g.27587652C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364785C>T , CM000664.2:g.27364785C>T	GRCh38
NC_000002.11:g.27587652C>T , CM000664.1:g.27587652C>T	GRCh37
NC_000002.10:g.27441156C>T	NCBI36
NG_009305.1:g.10673G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1305G>A (EIF2B4) MANE Select	ENSP00000233552.6:p.Leu435=
ENST00000347454.8:c.1305G>A (EIF2B4)	ENSP00000233552.5:p.Leu435=
ENST00000405940.6:c.*571G>A (EIF2B4)	ENSP00000384375.2:n.*571G>A
ENST00000445933.6:c.1302G>A (EIF2B4)	ENSP00000394397.2:p.Leu434=
ENST00000451130.6:c.1365G>A (EIF2B4)	ENSP00000394869.2:p.Leu455=
ENST00000478311.1:n.298G>A (EIF2B4)
ENST00000493344.6:c.1368G>A (EIF2B4)	ENSP00000429323.1:p.Leu456=
ENST00000616081.4:c.1296G>A (EIF2B4)	ENSP00000477710.1:p.Leu432=
ENST00000622434.4:c.*571G>A (EIF2B4)	ENSP00000479991.1:n.*571G>A
NM_001034116.1:c.1305G>A (EIF2B4)	NP_001029288.1:p.Leu435=
NM_015636.3:c.1302G>A (EIF2B4)	NP_056451.3:p.Leu434=
NM_172195.3:c.1365G>A (EIF2B4)	NP_751945.2:p.Leu455=
XM_005264632.1:c.1260G>A (EIF2B4)	XP_005264689.1:p.Leu420=
XM_006712132.1:c.1257G>A (EIF2B4)	XP_006712195.1:p.Leu419=
XM_011533147.1:c.687G>A (EIF2B4)	XP_011531449.1:p.Leu229=
XR_939868.1:n.1772-2639C>T (GTF3C2-AS2)
NM_001318965.1:c.1368G>A (EIF2B4)	NP_001305894.1:p.Leu456=
NM_001318966.1:c.1260G>A (EIF2B4)	NP_001305895.1:p.Leu420=
NM_001318967.1:c.1212G>A (EIF2B4)	NP_001305896.1:p.Leu404=
NM_001318968.1:c.720G>A (EIF2B4)	NP_001305897.1:p.Leu240=
NM_001318969.1:c.687G>A (EIF2B4)	NP_001305898.1:p.Leu229=
XM_011533147.2:c.687G>A (EIF2B4)	XP_011531449.1:p.Leu229=
NM_001034116.2:c.1305G>A (EIF2B4) MANE Select	NP_001029288.1:p.Leu435=
NM_001318965.2:c.1368G>A (EIF2B4)	NP_001305894.1:p.Leu456=
NM_001318966.2:c.1260G>A (EIF2B4)	NP_001305895.1:p.Leu420=
NM_001318967.2:c.1212G>A (EIF2B4)	NP_001305896.1:p.Leu404=
NM_001318968.2:c.720G>A (EIF2B4)	NP_001305897.1:p.Leu240=
NM_001318969.2:c.687G>A (EIF2B4)	NP_001305898.1:p.Leu229=
NM_015636.4:c.1302G>A (EIF2B4)	NP_056451.3:p.Leu434=
NM_172195.4:c.1365G>A (EIF2B4)	NP_751945.2:p.Leu455=