Canonical Allele Identifier: CA2147299419
Gene: EIF2B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005799C= , CM000676.2:g.75005799C= GRCh38
NC_000014.8:g.75472502C= , CM000676.1:g.75472502C= GRCh37
NC_000014.7:g.74542255C= NCBI36
NG_013333.1:g.7891C=

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.598-67C= MANE Select ENSP00000266126.5:n.598-67C=
ENST00000266126.9:c.598-67C= ENSP00000266126.5:n.598-67C=
ENST00000553401.5:c.571-42C= ENSP00000451681.1:n.571-42C=
ENST00000556028.5:c.598-98C= ENSP00000452311.1:n.598-98C=
NM_014239.3:c.598-67C= NP_055054.1:n.598-67C=
NM_014239.4:c.598-67C= MANE Select NP_055054.1:n.598-67C=
Search 100 bp 5'
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