Canonical Allele Identifier: CA390424254
Gene: EIF2B2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.293G>C MANE Select ENSP00000266126.5:p.Gly98Ala
ENST00000266126.9:c.293G>C ENSP00000266126.5:p.Gly98Ala
ENST00000553401.5:c.266G>C ENSP00000451681.1:p.Gly89Ala
ENST00000553539.1:n.588G>C
ENST00000555522.1:n.351G>C
ENST00000556028.5:c.293G>C ENSP00000452311.1:p.Gly98Ala
NM_014239.3:c.293G>C NP_055054.1:p.Gly98Ala
NM_014239.4:c.293G>C MANE Select NP_055054.1:p.Gly98Ala