Canonical Allele Identifier: CA390426367
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75472567A>T (hg19) chr14:g.75005864A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005864A>T , CM000676.2:g.75005864A>T GRCh38
NC_000014.8:g.75472567A>T , CM000676.1:g.75472567A>T GRCh37
NC_000014.7:g.74542320A>T NCBI36
NG_013333.1:g.7956A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.598-2A>T MANE Select ENSP00000266126.5:n.598-2A>T
ENST00000266126.9:c.598-2A>T ENSP00000266126.5:n.598-2A>T
ENST00000553401.5:c.594A>T ENSP00000451681.1:p.Ala198=
ENST00000556028.5:c.598-33A>T ENSP00000452311.1:n.598-33A>T
NM_014239.3:c.598-2A>T NP_055054.1:n.598-2A>T
NM_014239.4:c.598-2A>T MANE Select NP_055054.1:n.598-2A>T
Search 100 bp 5'
Search 100 bp 3'