Canonical Allele Identifier: CA1576636

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• ClinVar Variation Id: 2827153
• ClinVar RCV Id: RCV003683565
• dbSNP Id: rs760676299
• ExAC: 2:27589606 T / G
• gnomAD v2: 2-27589606-T-G
• gnomAD v4: 2-27366739-T-G
• MyVariant Identifiers: chr2:g.27589606T>G (hg19) ; chr2:g.27366739T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27366739T>G , CM000664.2:g.27366739T>G	GRCh38
NC_000002.11:g.27589606T>G , CM000664.1:g.27589606T>G	GRCh37
NC_000002.10:g.27443110T>G	NCBI36
NG_009305.1:g.8719A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1191+20A>C (EIF2B4) MANE Select	ENSP00000233552.6:n.1191+20A>C
ENST00000347454.8:c.1191+20A>C (EIF2B4)	ENSP00000233552.5:n.1191+20A>C
ENST00000405940.6:c.*457+20A>C (EIF2B4)	ENSP00000384375.2:n.*457+20A>C
ENST00000445933.6:c.1188+20A>C (EIF2B4)	ENSP00000394397.2:n.1188+20A>C
ENST00000451130.6:c.1251+20A>C (EIF2B4)	ENSP00000394869.2:n.1251+20A>C
ENST00000475582.5:n.3112A>C (EIF2B4)
ENST00000493344.6:c.1254+20A>C (EIF2B4)	ENSP00000429323.1:n.1254+20A>C
ENST00000616081.4:c.1182+20A>C (EIF2B4)	ENSP00000477710.1:n.1182+20A>C
ENST00000622434.4:c.*457+20A>C (EIF2B4)	ENSP00000479991.1:n.*457+20A>C
NM_001034116.1:c.1191+20A>C (EIF2B4)	NP_001029288.1:n.1191+20A>C
NM_015636.3:c.1188+20A>C (EIF2B4)	NP_056451.3:n.1188+20A>C
NM_172195.3:c.1251+20A>C (EIF2B4)	NP_751945.2:n.1251+20A>C
XM_005264632.1:c.1146+20A>C (EIF2B4)	XP_005264689.1:n.1146+20A>C
XM_006712132.1:c.1143+20A>C (EIF2B4)	XP_006712195.1:n.1143+20A>C
XM_011533147.1:c.573+20A>C (EIF2B4)	XP_011531449.1:n.573+20A>C
XR_939868.1:n.1772-685T>G (GTF3C2-AS2)
NM_001318965.1:c.1254+20A>C (EIF2B4)	NP_001305894.1:n.1254+20A>C
NM_001318966.1:c.1146+20A>C (EIF2B4)	NP_001305895.1:n.1146+20A>C
NM_001318967.1:c.1098+20A>C (EIF2B4)	NP_001305896.1:n.1098+20A>C
NM_001318968.1:c.606+20A>C (EIF2B4)	NP_001305897.1:n.606+20A>C
NM_001318969.1:c.573+20A>C (EIF2B4)	NP_001305898.1:n.573+20A>C
XM_011533147.2:c.573+20A>C (EIF2B4)	XP_011531449.1:n.573+20A>C
NM_001034116.2:c.1191+20A>C (EIF2B4) MANE Select	NP_001029288.1:n.1191+20A>C
NM_001318965.2:c.1254+20A>C (EIF2B4)	NP_001305894.1:n.1254+20A>C
NM_001318966.2:c.1146+20A>C (EIF2B4)	NP_001305895.1:n.1146+20A>C
NM_001318967.2:c.1098+20A>C (EIF2B4)	NP_001305896.1:n.1098+20A>C
NM_001318968.2:c.606+20A>C (EIF2B4)	NP_001305897.1:n.606+20A>C
NM_001318969.2:c.573+20A>C (EIF2B4)	NP_001305898.1:n.573+20A>C
NM_015636.4:c.1188+20A>C (EIF2B4)	NP_056451.3:n.1188+20A>C
NM_172195.4:c.1251+20A>C (EIF2B4)	NP_751945.2:n.1251+20A>C