Canonical Allele Identifier: CA390425822
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75471492T>A (hg19) chr14:g.75004789T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75004789T>A , CM000676.2:g.75004789T>A GRCh38
NC_000014.8:g.75471492T>A , CM000676.1:g.75471492T>A GRCh37
NC_000014.7:g.74541245T>A NCBI36
NG_013333.1:g.6881T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.486T>A MANE Select ENSP00000266126.5:p.Asn162Lys
ENST00000266126.9:c.486T>A ENSP00000266126.5:p.Asn162Lys
ENST00000553401.5:c.459T>A ENSP00000451681.1:p.Asn153Lys
ENST00000553539.1:n.781T>A
ENST00000555522.1:n.544T>A
ENST00000556028.5:c.486T>A ENSP00000452311.1:p.Asn162Lys
NM_014239.3:c.486T>A NP_055054.1:p.Asn162Lys
NM_014239.4:c.486T>A MANE Select NP_055054.1:p.Asn162Lys
Search 100 bp 5'
Search 100 bp 3'