Canonical Allele Identifier: CA390424253
Gene: EIF2B2 HGNC NCBI

Linked Data

COSMIC: COSM3793864
MyVariant Identifiers: chr14:g.75470262G>A (hg19) chr14:g.75003559G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75003559G>A , CM000676.2:g.75003559G>A GRCh38
NC_000014.8:g.75470262G>A , CM000676.1:g.75470262G>A GRCh37
NC_000014.7:g.74540015G>A NCBI36
NG_013333.1:g.5651G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.293G>A MANE Select ENSP00000266126.5:p.Gly98Glu
ENST00000266126.9:c.293G>A ENSP00000266126.5:p.Gly98Glu
ENST00000553401.5:c.266G>A ENSP00000451681.1:p.Gly89Glu
ENST00000553539.1:n.588G>A
ENST00000555522.1:n.351G>A
ENST00000556028.5:c.293G>A ENSP00000452311.1:p.Gly98Glu
NM_014239.3:c.293G>A NP_055054.1:p.Gly98Glu
NM_014239.4:c.293G>A MANE Select NP_055054.1:p.Gly98Glu
Search 100 bp 5'
Search 100 bp 3'