Canonical Allele Identifier: CA2147299384
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005676G= , CM000676.2:g.75005676G= GRCh38
NC_000014.8:g.75472379G= , CM000676.1:g.75472379G= GRCh37
NC_000014.7:g.74542132G= NCBI36
NG_013333.1:g.7768G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.598-190G= MANE Select ENSP00000266126.5:n.598-190G=
ENST00000266126.9:c.598-190G= ENSP00000266126.5:n.598-190G=
ENST00000553401.5:c.571-165G= ENSP00000451681.1:n.571-165G=
ENST00000556028.5:c.598-221G= ENSP00000452311.1:n.598-221G=
NM_014239.3:c.598-190G= NP_055054.1:n.598-190G=
NM_014239.4:c.598-190G= MANE Select NP_055054.1:n.598-190G=