Canonical Allele Identifier: CA2147298378

Gene: EIF2B2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75003557T= , CM000676.2:g.75003557T=	GRCh38
NC_000014.8:g.75470260T= , CM000676.1:g.75470260T=	GRCh37
NC_000014.7:g.74540013T=	NCBI36
NG_013333.1:g.5649T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266126.10:c.291T= MANE Select	ENSP00000266126.5:p.His97=
ENST00000266126.9:c.291T=	ENSP00000266126.5:p.His97=
ENST00000553401.5:c.264T=	ENSP00000451681.1:p.His88=
ENST00000553539.1:n.586T=
ENST00000555522.1:n.349T=
ENST00000556028.5:c.291T=	ENSP00000452311.1:p.His97=
NM_014239.3:c.291T=	NP_055054.1:p.His97=
NM_014239.4:c.291T= MANE Select	NP_055054.1:p.His97=