Canonical Allele Identifier: CA390430007
Gene: EIF2B2 HGNC NCBI

Linked Data

dbSNP Id: rs113994018

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75009042G>A , CM000676.2:g.75009042G>A GRCh38
NC_000014.8:g.75475745G>A , CM000676.1:g.75475745G>A GRCh37
NC_000014.7:g.74545498G>A NCBI36
NG_013333.1:g.11134G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.910G>A MANE Select ENSP00000266126.5:p.Glu304Lys
ENST00000266126.9:c.910G>A ENSP00000266126.5:p.Glu304Lys
ENST00000556668.1:n.490G>A
NM_014239.3:c.910G>A NP_055054.1:p.Glu304Lys
NM_014239.4:c.910G>A MANE Select NP_055054.1:p.Glu304Lys