Canonical Allele Identifier: CA2147299428
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005820A= , CM000676.2:g.75005820A= GRCh38
NC_000014.8:g.75472523A= , CM000676.1:g.75472523A= GRCh37
NC_000014.7:g.74542276A= NCBI36
NG_013333.1:g.7912A=

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.598-46A= MANE Select ENSP00000266126.5:n.598-46A=
ENST00000266126.9:c.598-46A= ENSP00000266126.5:n.598-46A=
ENST00000553401.5:c.571-21A= ENSP00000451681.1:n.571-21A=
ENST00000556028.5:c.598-77A= ENSP00000452311.1:n.598-77A=
NM_014239.3:c.598-46A= NP_055054.1:n.598-46A=
NM_014239.4:c.598-46A= MANE Select NP_055054.1:n.598-46A=