Canonical Allele Identifier: CA346196799

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• dbSNP Id: rs2148368012
• MyVariant Identifiers: chr2:g.27587460G>T (hg19) ; chr2:g.27364593G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364593G>T , CM000664.2:g.27364593G>T	GRCh38
NC_000002.11:g.27587460G>T , CM000664.1:g.27587460G>T	GRCh37
NC_000002.10:g.27440964G>T	NCBI36
NG_009305.1:g.10865C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1379C>A (EIF2B4) MANE Select	ENSP00000233552.6:p.Pro460His
ENST00000347454.8:c.1379C>A (EIF2B4)	ENSP00000233552.5:p.Pro460His
ENST00000405940.6:c.*645C>A (EIF2B4)	ENSP00000384375.2:n.*645C>A
ENST00000445933.6:c.1376C>A (EIF2B4)	ENSP00000394397.2:p.Pro459His
ENST00000451130.6:c.1439C>A (EIF2B4)	ENSP00000394869.2:p.Pro480His
ENST00000478311.1:n.372C>A (EIF2B4)
ENST00000493344.6:c.1442C>A (EIF2B4)	ENSP00000429323.1:p.Pro481His
ENST00000616081.4:c.1370C>A (EIF2B4)	ENSP00000477710.1:p.Pro457His
ENST00000622434.4:c.*645C>A (EIF2B4)	ENSP00000479991.1:n.*645C>A
NM_001034116.1:c.1379C>A (EIF2B4)	NP_001029288.1:p.Pro460His
NM_015636.3:c.1376C>A (EIF2B4)	NP_056451.3:p.Pro459His
NM_172195.3:c.1439C>A (EIF2B4)	NP_751945.2:p.Pro480His
XM_005264632.1:c.1334C>A (EIF2B4)	XP_005264689.1:p.Pro445His
XM_006712132.1:c.1331C>A (EIF2B4)	XP_006712195.1:p.Pro444His
XM_011533147.1:c.761C>A (EIF2B4)	XP_011531449.1:p.Pro254His
XR_939868.1:n.1772-2831G>T (GTF3C2-AS2)
NM_001318965.1:c.1442C>A (EIF2B4)	NP_001305894.1:p.Pro481His
NM_001318966.1:c.1334C>A (EIF2B4)	NP_001305895.1:p.Pro445His
NM_001318967.1:c.1286C>A (EIF2B4)	NP_001305896.1:p.Pro429His
NM_001318968.1:c.794C>A (EIF2B4)	NP_001305897.1:p.Pro265His
NM_001318969.1:c.761C>A (EIF2B4)	NP_001305898.1:p.Pro254His
XM_011533147.2:c.761C>A (EIF2B4)	XP_011531449.1:p.Pro254His
NM_001034116.2:c.1379C>A (EIF2B4) MANE Select	NP_001029288.1:p.Pro460His
NM_001318965.2:c.1442C>A (EIF2B4)	NP_001305894.1:p.Pro481His
NM_001318966.2:c.1334C>A (EIF2B4)	NP_001305895.1:p.Pro445His
NM_001318967.2:c.1286C>A (EIF2B4)	NP_001305896.1:p.Pro429His
NM_001318968.2:c.794C>A (EIF2B4)	NP_001305897.1:p.Pro265His
NM_001318969.2:c.761C>A (EIF2B4)	NP_001305898.1:p.Pro254His
NM_015636.4:c.1376C>A (EIF2B4)	NP_056451.3:p.Pro459His
NM_172195.4:c.1439C>A (EIF2B4)	NP_751945.2:p.Pro480His