Canonical Allele Identifier: CA346197916

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• gnomAD v4: 2-27366838-T-G
• MyVariant Identifiers: chr2:g.27589705T>G (hg19) ; chr2:g.27366838T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27366838T>G , CM000664.2:g.27366838T>G	GRCh38
NC_000002.11:g.27589705T>G , CM000664.1:g.27589705T>G	GRCh37
NC_000002.10:g.27443209T>G	NCBI36
NG_009305.1:g.8620A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1112A>C (EIF2B4) MANE Select	ENSP00000233552.6:p.His371Pro
ENST00000347454.8:c.1112A>C (EIF2B4)	ENSP00000233552.5:p.His371Pro
ENST00000405940.6:c.*378A>C (EIF2B4)	ENSP00000384375.2:n.*378A>C
ENST00000417567.1:c.686A>C (EIF2B4)
ENST00000445933.6:c.1109A>C (EIF2B4)	ENSP00000394397.2:p.His370Pro
ENST00000451130.6:c.1172A>C (EIF2B4)	ENSP00000394869.2:p.His391Pro
ENST00000475582.5:n.3013A>C (EIF2B4)
ENST00000493344.6:c.1175A>C (EIF2B4)	ENSP00000429323.1:p.His392Pro
ENST00000616081.4:c.1103A>C (EIF2B4)	ENSP00000477710.1:p.His368Pro
ENST00000622434.4:c.*378A>C (EIF2B4)	ENSP00000479991.1:n.*378A>C
NM_001034116.1:c.1112A>C (EIF2B4)	NP_001029288.1:p.His371Pro
NM_015636.3:c.1109A>C (EIF2B4)	NP_056451.3:p.His370Pro
NM_172195.3:c.1172A>C (EIF2B4)	NP_751945.2:p.His391Pro
XM_005264632.1:c.1067A>C (EIF2B4)	XP_005264689.1:p.His356Pro
XM_006712132.1:c.1064A>C (EIF2B4)	XP_006712195.1:p.His355Pro
XM_011533147.1:c.494A>C (EIF2B4)	XP_011531449.1:p.His165Pro
XR_939868.1:n.1772-586T>G (GTF3C2-AS2)
NM_001318965.1:c.1175A>C (EIF2B4)	NP_001305894.1:p.His392Pro
NM_001318966.1:c.1067A>C (EIF2B4)	NP_001305895.1:p.His356Pro
NM_001318967.1:c.1019A>C (EIF2B4)	NP_001305896.1:p.His340Pro
NM_001318968.1:c.527A>C (EIF2B4)	NP_001305897.1:p.His176Pro
NM_001318969.1:c.494A>C (EIF2B4)	NP_001305898.1:p.His165Pro
XM_011533147.2:c.494A>C (EIF2B4)	XP_011531449.1:p.His165Pro
NM_001034116.2:c.1112A>C (EIF2B4) MANE Select	NP_001029288.1:p.His371Pro
NM_001318965.2:c.1175A>C (EIF2B4)	NP_001305894.1:p.His392Pro
NM_001318966.2:c.1067A>C (EIF2B4)	NP_001305895.1:p.His356Pro
NM_001318967.2:c.1019A>C (EIF2B4)	NP_001305896.1:p.His340Pro
NM_001318968.2:c.527A>C (EIF2B4)	NP_001305897.1:p.His176Pro
NM_001318969.2:c.494A>C (EIF2B4)	NP_001305898.1:p.His165Pro
NM_015636.4:c.1109A>C (EIF2B4)	NP_056451.3:p.His370Pro
NM_172195.4:c.1172A>C (EIF2B4)	NP_751945.2:p.His391Pro