Canonical Allele Identifier: CA2147298233
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75003246C= , CM000676.2:g.75003246C= GRCh38
NC_000014.8:g.75469949C= , CM000676.1:g.75469949C= GRCh37
NC_000014.7:g.74539702C= NCBI36
NG_013333.1:g.5338C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.164-29C= MANE Select ENSP00000266126.5:n.164-29C=
ENST00000266126.9:c.164-29C= ENSP00000266126.5:n.164-29C=
ENST00000553401.5:c.137-29C= ENSP00000451681.1:n.137-29C=
ENST00000553539.1:n.275C=
ENST00000555522.1:n.222-29C=
ENST00000556028.5:c.164-29C= ENSP00000452311.1:n.164-29C=
NM_014239.3:c.164-29C= NP_055054.1:n.164-29C=
NM_014239.4:c.164-29C= MANE Select NP_055054.1:n.164-29C=