Canonical Allele Identifier: CA390429953
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75475733G>A (hg19) chr14:g.75009030G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75009030G>A , CM000676.2:g.75009030G>A GRCh38
NC_000014.8:g.75475733G>A , CM000676.1:g.75475733G>A GRCh37
NC_000014.7:g.74545486G>A NCBI36
NG_013333.1:g.11122G>A

Transcript Alleles

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