Canonical Allele Identifier: CA2147299439
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005852C= , CM000676.2:g.75005852C= GRCh38
NC_000014.8:g.75472555C= , CM000676.1:g.75472555C= GRCh37
NC_000014.7:g.74542308C= NCBI36
NG_013333.1:g.7944C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.598-14C= MANE Select ENSP00000266126.5:n.598-14C=
ENST00000266126.9:c.598-14C= ENSP00000266126.5:n.598-14C=
ENST00000553401.5:c.582C= ENSP00000451681.1:p.Phe194=
ENST00000556028.5:c.598-45C= ENSP00000452311.1:n.598-45C=
NM_014239.3:c.598-14C= NP_055054.1:n.598-14C=
NM_014239.4:c.598-14C= MANE Select NP_055054.1:n.598-14C=