Canonical Allele Identifier: CA2147299402
Gene: EIF2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005738T= , CM000676.2:g.75005738T= GRCh38
NC_000014.8:g.75472441T= , CM000676.1:g.75472441T= GRCh37
NC_000014.7:g.74542194T= NCBI36
NG_013333.1:g.7830T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.598-128T= MANE Select ENSP00000266126.5:n.598-128T=
ENST00000266126.9:c.598-128T= ENSP00000266126.5:n.598-128T=
ENST00000553401.5:c.571-103T= ENSP00000451681.1:n.571-103T=
ENST00000556028.5:c.598-159T= ENSP00000452311.1:n.598-159T=
NM_014239.3:c.598-128T= NP_055054.1:n.598-128T=
NM_014239.4:c.598-128T= MANE Select NP_055054.1:n.598-128T=