Canonical Allele Identifier: CA390426628
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75472627A>G (hg19) chr14:g.75005924A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005924A>G , CM000676.2:g.75005924A>G GRCh38
NC_000014.8:g.75472627A>G , CM000676.1:g.75472627A>G GRCh37
NC_000014.7:g.74542380A>G NCBI36
NG_013333.1:g.8016A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.656A>G MANE Select ENSP00000266126.5:p.Asp219Gly
ENST00000266126.9:c.656A>G ENSP00000266126.5:p.Asp219Gly
ENST00000553401.5:c.654A>G ENSP00000451681.1:n.654A>G
ENST00000554748.2:c.20A>G ENSP00000452582.2:p.Asp7Gly
ENST00000556028.5:c.*4A>G ENSP00000452311.1:n.*4A>G
NM_014239.3:c.656A>G NP_055054.1:p.Asp219Gly
NM_014239.4:c.656A>G MANE Select NP_055054.1:p.Asp219Gly
Search 100 bp 5'
Search 100 bp 3'