Canonical Allele Identifier: CA2147298368
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75003539T= , CM000676.2:g.75003539T= GRCh38
NC_000014.8:g.75470242T= , CM000676.1:g.75470242T= GRCh37
NC_000014.7:g.74539995T= NCBI36
NG_013333.1:g.5631T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.285-12T= MANE Select ENSP00000266126.5:n.285-12T=
ENST00000266126.9:c.285-12T= ENSP00000266126.5:n.285-12T=
ENST00000553401.5:c.258-12T= ENSP00000451681.1:n.258-12T=
ENST00000553539.1:n.568T=
ENST00000555522.1:n.343-12T=
ENST00000556028.5:c.285-12T= ENSP00000452311.1:n.285-12T=
NM_014239.3:c.285-12T= NP_055054.1:n.285-12T=
NM_014239.4:c.285-12T= MANE Select NP_055054.1:n.285-12T=