Canonical Allele Identifier: CA2147298377
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75003551A= , CM000676.2:g.75003551A= GRCh38
NC_000014.8:g.75470254A= , CM000676.1:g.75470254A= GRCh37
NC_000014.7:g.74540007A= NCBI36
NG_013333.1:g.5643A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.285A= MANE Select ENSP00000266126.5:p.Arg95=
ENST00000266126.9:c.285A= ENSP00000266126.5:p.Arg95=
ENST00000553401.5:c.258A= ENSP00000451681.1:p.Arg86=
ENST00000553539.1:n.580A=
ENST00000555522.1:n.343A=
ENST00000556028.5:c.285A= ENSP00000452311.1:p.Arg95=
NM_014239.3:c.285A= NP_055054.1:p.Arg95=
NM_014239.4:c.285A= MANE Select NP_055054.1:p.Arg95=