Canonical Allele Identifier: CA425410061
Gene: EIF2B4 HGNC NCBI
GTF3C2-AS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.27587613C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27364746C>T , CM000664.2:g.27364746C>T GRCh38
NC_000002.11:g.27587613C>T , CM000664.1:g.27587613C>T GRCh37
NC_000002.10:g.27441117C>T NCBI36
NG_009305.1:g.10712G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347454.9:c.1344G>A (EIF2B4) MANE Select ENSP00000233552.6:p.Gln448=
ENST00000347454.8:c.1344G>A (EIF2B4) ENSP00000233552.5:p.Gln448=
ENST00000405940.6:c.*610G>A (EIF2B4) ENSP00000384375.2:n.*610G>A
ENST00000445933.6:c.1341G>A (EIF2B4) ENSP00000394397.2:p.Gln447=
ENST00000451130.6:c.1404G>A (EIF2B4) ENSP00000394869.2:p.Gln468=
ENST00000478311.1:n.337G>A (EIF2B4)
ENST00000493344.6:c.1407G>A (EIF2B4) ENSP00000429323.1:p.Gln469=
ENST00000616081.4:c.1335G>A (EIF2B4) ENSP00000477710.1:p.Gln445=
ENST00000622434.4:c.*610G>A (EIF2B4) ENSP00000479991.1:n.*610G>A
NM_001034116.1:c.1344G>A (EIF2B4) NP_001029288.1:p.Gln448=
NM_015636.3:c.1341G>A (EIF2B4) NP_056451.3:p.Gln447=
NM_172195.3:c.1404G>A (EIF2B4) NP_751945.2:p.Gln468=
XM_005264632.1:c.1299G>A (EIF2B4) XP_005264689.1:p.Gln433=
XM_006712132.1:c.1296G>A (EIF2B4) XP_006712195.1:p.Gln432=
XM_011533147.1:c.726G>A (EIF2B4) XP_011531449.1:p.Gln242=
XR_939868.1:n.1772-2678C>T (GTF3C2-AS2)
NM_001318965.1:c.1407G>A (EIF2B4) NP_001305894.1:p.Gln469=
NM_001318966.1:c.1299G>A (EIF2B4) NP_001305895.1:p.Gln433=
NM_001318967.1:c.1251G>A (EIF2B4) NP_001305896.1:p.Gln417=
NM_001318968.1:c.759G>A (EIF2B4) NP_001305897.1:p.Gln253=
NM_001318969.1:c.726G>A (EIF2B4) NP_001305898.1:p.Gln242=
XM_011533147.2:c.726G>A (EIF2B4) XP_011531449.1:p.Gln242=
NM_001034116.2:c.1344G>A (EIF2B4) MANE Select NP_001029288.1:p.Gln448=
NM_001318965.2:c.1407G>A (EIF2B4) NP_001305894.1:p.Gln469=
NM_001318966.2:c.1299G>A (EIF2B4) NP_001305895.1:p.Gln433=
NM_001318967.2:c.1251G>A (EIF2B4) NP_001305896.1:p.Gln417=
NM_001318968.2:c.759G>A (EIF2B4) NP_001305897.1:p.Gln253=
NM_001318969.2:c.726G>A (EIF2B4) NP_001305898.1:p.Gln242=
NM_015636.4:c.1341G>A (EIF2B4) NP_056451.3:p.Gln447=
NM_172195.4:c.1404G>A (EIF2B4) NP_751945.2:p.Gln468=