Canonical Allele Identifier: CA2147299446

Gene: EIF2B2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75005866G= , CM000676.2:g.75005866G=	GRCh38
NC_000014.8:g.75472569G= , CM000676.1:g.75472569G=	GRCh37
NC_000014.7:g.74542322G=	NCBI36
NG_013333.1:g.7958G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266126.10:c.598G= MANE Select	ENSP00000266126.5:p.Gly200=
ENST00000266126.9:c.598G=	ENSP00000266126.5:p.Gly200=
ENST00000553401.5:c.596G=	ENSP00000451681.1:p.Gly199=
ENST00000556028.5:c.598-31G=	ENSP00000452311.1:n.598-31G=
NM_014239.3:c.598G=	NP_055054.1:p.Gly200=
NM_014239.4:c.598G= MANE Select	NP_055054.1:p.Gly200=