Canonical Allele Identifier: CA2147298345
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75003497A= , CM000676.2:g.75003497A= GRCh38
NC_000014.8:g.75470200A= , CM000676.1:g.75470200A= GRCh37
NC_000014.7:g.74539953A= NCBI36
NG_013333.1:g.5589A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.285-54A= MANE Select ENSP00000266126.5:n.285-54A=
ENST00000266126.9:c.285-54A= ENSP00000266126.5:n.285-54A=
ENST00000553401.5:c.258-54A= ENSP00000451681.1:n.258-54A=
ENST00000553539.1:n.526A=
ENST00000555522.1:n.343-54A=
ENST00000556028.5:c.285-54A= ENSP00000452311.1:n.285-54A=
NM_014239.3:c.285-54A= NP_055054.1:n.285-54A=
NM_014239.4:c.285-54A= MANE Select NP_055054.1:n.285-54A=