Canonical Allele Identifier: CA487178838
Gene: EIF2B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75475786C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75009083C>G , CM000676.2:g.75009083C>G GRCh38
NC_000014.8:g.75475786C>G , CM000676.1:g.75475786C>G GRCh37
NC_000014.7:g.74545539C>G NCBI36
NG_013333.1:g.11175C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.951C>G MANE Select ENSP00000266126.5:p.Pro317=
ENST00000266126.9:c.951C>G ENSP00000266126.5:p.Pro317=
ENST00000556668.1:n.531C>G
NM_014239.3:c.951C>G NP_055054.1:p.Pro317=
NM_014239.4:c.951C>G MANE Select NP_055054.1:p.Pro317=
Search 100 bp 5'
Search 100 bp 3'