Canonical Allele Identifier: CA390424250
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75470261G>C (hg19) chr14:g.75003558G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75003558G>C , CM000676.2:g.75003558G>C GRCh38
NC_000014.8:g.75470261G>C , CM000676.1:g.75470261G>C GRCh37
NC_000014.7:g.74540014G>C NCBI36
NG_013333.1:g.5650G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.292G>C MANE Select ENSP00000266126.5:p.Gly98Arg
ENST00000266126.9:c.292G>C ENSP00000266126.5:p.Gly98Arg
ENST00000553401.5:c.265G>C ENSP00000451681.1:p.Gly89Arg
ENST00000553539.1:n.587G>C
ENST00000555522.1:n.350G>C
ENST00000556028.5:c.292G>C ENSP00000452311.1:p.Gly98Arg
NM_014239.3:c.292G>C NP_055054.1:p.Gly98Arg
NM_014239.4:c.292G>C MANE Select NP_055054.1:p.Gly98Arg
Search 100 bp 5'
Search 100 bp 3'