Canonical Allele Identifier: CA2147300725
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75009053C= , CM000676.2:g.75009053C= GRCh38
NC_000014.8:g.75475756C= , CM000676.1:g.75475756C= GRCh37
NC_000014.7:g.74545509C= NCBI36
NG_013333.1:g.11145C=

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.921C= MANE Select ENSP00000266126.5:p.Ser307=
ENST00000266126.9:c.921C= ENSP00000266126.5:p.Ser307=
ENST00000556668.1:n.501C=
NM_014239.3:c.921C= NP_055054.1:p.Ser307=
NM_014239.4:c.921C= MANE Select NP_055054.1:p.Ser307=