Canonical Allele Identifier: CA2147298229

Gene: EIF2B2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75003236C= , CM000676.2:g.75003236C=	GRCh38
NC_000014.8:g.75469939C= , CM000676.1:g.75469939C=	GRCh37
NC_000014.7:g.74539692C=	NCBI36
NG_013333.1:g.5328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266126.10:c.164-39C= MANE Select	ENSP00000266126.5:n.164-39C=
ENST00000266126.9:c.164-39C=	ENSP00000266126.5:n.164-39C=
ENST00000553401.5:c.137-39C=	ENSP00000451681.1:n.137-39C=
ENST00000553539.1:n.265C=
ENST00000555522.1:n.222-39C=
ENST00000556028.5:c.164-39C=	ENSP00000452311.1:n.164-39C=
NM_014239.3:c.164-39C=	NP_055054.1:n.164-39C=
NM_014239.4:c.164-39C= MANE Select	NP_055054.1:n.164-39C=