Canonical Allele Identifier: CA1240242881

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• dbSNP Id: rs1681711529

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364668C>A , CM000664.2:g.27364668C>A	GRCh38
NC_000002.11:g.27587535C>A , CM000664.1:g.27587535C>A	GRCh37
NC_000002.10:g.27441039C>A	NCBI36
NG_009305.1:g.10790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1372+50G>T (EIF2B4) MANE Select	ENSP00000233552.6:n.1372+50G>T
ENST00000347454.8:c.1372+50G>T (EIF2B4)	ENSP00000233552.5:n.1372+50G>T
ENST00000405940.6:c.*638+50G>T (EIF2B4)	ENSP00000384375.2:n.*638+50G>T
ENST00000445933.6:c.1369+50G>T (EIF2B4)	ENSP00000394397.2:n.1369+50G>T
ENST00000451130.6:c.1432+50G>T (EIF2B4)	ENSP00000394869.2:n.1432+50G>T
ENST00000478311.1:n.365+50G>T (EIF2B4)
ENST00000493344.6:c.1435+50G>T (EIF2B4)	ENSP00000429323.1:n.1435+50G>T
ENST00000616081.4:c.1363+50G>T (EIF2B4)	ENSP00000477710.1:n.1363+50G>T
ENST00000622434.4:c.*638+50G>T (EIF2B4)	ENSP00000479991.1:n.*638+50G>T
NM_001034116.1:c.1372+50G>T (EIF2B4)	NP_001029288.1:n.1372+50G>T
NM_015636.3:c.1369+50G>T (EIF2B4)	NP_056451.3:n.1369+50G>T
NM_172195.3:c.1432+50G>T (EIF2B4)	NP_751945.2:n.1432+50G>T
XM_005264632.1:c.1327+50G>T (EIF2B4)	XP_005264689.1:n.1327+50G>T
XM_006712132.1:c.1324+50G>T (EIF2B4)	XP_006712195.1:n.1324+50G>T
XM_011533147.1:c.754+50G>T (EIF2B4)	XP_011531449.1:n.754+50G>T
XR_939868.1:n.1772-2756C>A (GTF3C2-AS2)
NM_001318965.1:c.1435+50G>T (EIF2B4)	NP_001305894.1:n.1435+50G>T
NM_001318966.1:c.1327+50G>T (EIF2B4)	NP_001305895.1:n.1327+50G>T
NM_001318967.1:c.1279+50G>T (EIF2B4)	NP_001305896.1:n.1279+50G>T
NM_001318968.1:c.787+50G>T (EIF2B4)	NP_001305897.1:n.787+50G>T
NM_001318969.1:c.754+50G>T (EIF2B4)	NP_001305898.1:n.754+50G>T
XM_011533147.2:c.754+50G>T (EIF2B4)	XP_011531449.1:n.754+50G>T
NM_001034116.2:c.1372+50G>T (EIF2B4) MANE Select	NP_001029288.1:n.1372+50G>T
NM_001318965.2:c.1435+50G>T (EIF2B4)	NP_001305894.1:n.1435+50G>T
NM_001318966.2:c.1327+50G>T (EIF2B4)	NP_001305895.1:n.1327+50G>T
NM_001318967.2:c.1279+50G>T (EIF2B4)	NP_001305896.1:n.1279+50G>T
NM_001318968.2:c.787+50G>T (EIF2B4)	NP_001305897.1:n.787+50G>T
NM_001318969.2:c.754+50G>T (EIF2B4)	NP_001305898.1:n.754+50G>T
NM_015636.4:c.1369+50G>T (EIF2B4)	NP_056451.3:n.1369+50G>T
NM_172195.4:c.1432+50G>T (EIF2B4)	NP_751945.2:n.1432+50G>T