Canonical Allele Identifier: CA425410264

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587679C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364812C>G , CM000664.2:g.27364812C>G	GRCh38
NC_000002.11:g.27587679C>G , CM000664.1:g.27587679C>G	GRCh37
NC_000002.10:g.27441183C>G	NCBI36
NG_009305.1:g.10646G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1278G>C (EIF2B4) MANE Select	ENSP00000233552.6:p.Val426=
ENST00000347454.8:c.1278G>C (EIF2B4)	ENSP00000233552.5:p.Val426=
ENST00000405940.6:c.*544G>C (EIF2B4)	ENSP00000384375.2:n.*544G>C
ENST00000445933.6:c.1275G>C (EIF2B4)	ENSP00000394397.2:p.Val425=
ENST00000451130.6:c.1338G>C (EIF2B4)	ENSP00000394869.2:p.Val446=
ENST00000478311.1:n.271G>C (EIF2B4)
ENST00000493344.6:c.1341G>C (EIF2B4)	ENSP00000429323.1:p.Val447=
ENST00000616081.4:c.1269G>C (EIF2B4)	ENSP00000477710.1:p.Val423=
ENST00000622434.4:c.*544G>C (EIF2B4)	ENSP00000479991.1:n.*544G>C
NM_001034116.1:c.1278G>C (EIF2B4)	NP_001029288.1:p.Val426=
NM_015636.3:c.1275G>C (EIF2B4)	NP_056451.3:p.Val425=
NM_172195.3:c.1338G>C (EIF2B4)	NP_751945.2:p.Val446=
XM_005264632.1:c.1233G>C (EIF2B4)	XP_005264689.1:p.Val411=
XM_006712132.1:c.1230G>C (EIF2B4)	XP_006712195.1:p.Val410=
XM_011533147.1:c.660G>C (EIF2B4)	XP_011531449.1:p.Val220=
XR_939868.1:n.1772-2612C>G (GTF3C2-AS2)
NM_001318965.1:c.1341G>C (EIF2B4)	NP_001305894.1:p.Val447=
NM_001318966.1:c.1233G>C (EIF2B4)	NP_001305895.1:p.Val411=
NM_001318967.1:c.1185G>C (EIF2B4)	NP_001305896.1:p.Val395=
NM_001318968.1:c.693G>C (EIF2B4)	NP_001305897.1:p.Val231=
NM_001318969.1:c.660G>C (EIF2B4)	NP_001305898.1:p.Val220=
XM_011533147.2:c.660G>C (EIF2B4)	XP_011531449.1:p.Val220=
NM_001034116.2:c.1278G>C (EIF2B4) MANE Select	NP_001029288.1:p.Val426=
NM_001318965.2:c.1341G>C (EIF2B4)	NP_001305894.1:p.Val447=
NM_001318966.2:c.1233G>C (EIF2B4)	NP_001305895.1:p.Val411=
NM_001318967.2:c.1185G>C (EIF2B4)	NP_001305896.1:p.Val395=
NM_001318968.2:c.693G>C (EIF2B4)	NP_001305897.1:p.Val231=
NM_001318969.2:c.660G>C (EIF2B4)	NP_001305898.1:p.Val220=
NM_015636.4:c.1275G>C (EIF2B4)	NP_056451.3:p.Val425=
NM_172195.4:c.1338G>C (EIF2B4)	NP_751945.2:p.Val446=