Canonical Allele Identifier: CA2147300726
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75009054G= , CM000676.2:g.75009054G= GRCh38
NC_000014.8:g.75475757G= , CM000676.1:g.75475757G= GRCh37
NC_000014.7:g.74545510G= NCBI36
NG_013333.1:g.11146G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.922G= MANE Select ENSP00000266126.5:p.Val308=
ENST00000266126.9:c.922G= ENSP00000266126.5:p.Val308=
ENST00000556668.1:n.502G=
NM_014239.3:c.922G= NP_055054.1:p.Val308=
NM_014239.4:c.922G= MANE Select NP_055054.1:p.Val308=