Canonical Allele Identifier: CA2625725428
Gene: EIF2B2 HGNC NCBI

Linked Data

gnomAD v4: 14-75008980-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75008980A>G , CM000676.2:g.75008980A>G GRCh38
NC_000014.8:g.75475683A>G , CM000676.1:g.75475683A>G GRCh37
NC_000014.7:g.74545436A>G NCBI36
NG_013333.1:g.11072A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.899-51A>G MANE Select ENSP00000266126.5:n.899-51A>G
ENST00000266126.9:c.899-51A>G ENSP00000266126.5:n.899-51A>G
ENST00000556668.1:n.479-51A>G
NM_014239.3:c.899-51A>G NP_055054.1:n.899-51A>G
NM_014239.4:c.899-51A>G MANE Select NP_055054.1:n.899-51A>G
Search 100 bp 5'
Search 100 bp 3'