Canonical Allele Identifier: CA2147299413

Gene: EIF2B2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75005773A= , CM000676.2:g.75005773A=	GRCh38
NC_000014.8:g.75472476A= , CM000676.1:g.75472476A=	GRCh37
NC_000014.7:g.74542229A=	NCBI36
NG_013333.1:g.7865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266126.10:c.598-93A= MANE Select	ENSP00000266126.5:n.598-93A=
ENST00000266126.9:c.598-93A=	ENSP00000266126.5:n.598-93A=
ENST00000553401.5:c.571-68A=	ENSP00000451681.1:n.571-68A=
ENST00000556028.5:c.598-124A=	ENSP00000452311.1:n.598-124A=
NM_014239.3:c.598-93A=	NP_055054.1:n.598-93A=
NM_014239.4:c.598-93A= MANE Select	NP_055054.1:n.598-93A=