Canonical Allele Identifier: CA390429104
Gene: EIF2B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1414727
ClinVar RCV Id: RCV001930616
dbSNP Id: rs113994016

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75006701A>T , CM000676.2:g.75006701A>T GRCh38
NC_000014.8:g.75473404A>T , CM000676.1:g.75473404A>T GRCh37
NC_000014.7:g.74543157A>T NCBI36
NG_013333.1:g.8793A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.818A>T MANE Select ENSP00000266126.5:p.Lys273Ile
ENST00000266126.9:c.818A>T ENSP00000266126.5:p.Lys273Ile
ENST00000553401.5:c.816A>T ENSP00000451681.1:n.816A>T
ENST00000554748.2:c.182A>T ENSP00000452582.2:p.Lys61Ile
ENST00000556028.5:c.*166A>T ENSP00000452311.1:n.*166A>T
ENST00000556668.1:n.398A>T
NM_014239.3:c.818A>T NP_055054.1:p.Lys273Ile
NM_014239.4:c.818A>T MANE Select NP_055054.1:p.Lys273Ile