Canonical Allele Identifier: CA390429949
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75475732A>T (hg19) chr14:g.75009029A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75009029A>T , CM000676.2:g.75009029A>T GRCh38
NC_000014.8:g.75475732A>T , CM000676.1:g.75475732A>T GRCh37
NC_000014.7:g.74545485A>T NCBI36
NG_013333.1:g.11121A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.899-2A>T MANE Select ENSP00000266126.5:n.899-2A>T
ENST00000266126.9:c.899-2A>T ENSP00000266126.5:n.899-2A>T
ENST00000556668.1:n.479-2A>T
NM_014239.3:c.899-2A>T NP_055054.1:n.899-2A>T
NM_014239.4:c.899-2A>T MANE Select NP_055054.1:n.899-2A>T
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