Canonical Allele Identifier: CA708574168
Gene: EIF2B2 HGNC NCBI

Linked Data

dbSNP Id: rs771416034

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75005810A>G , CM000676.2:g.75005810A>G GRCh38
NC_000014.8:g.75472513A>G , CM000676.1:g.75472513A>G GRCh37
NC_000014.7:g.74542266A>G NCBI36
NG_013333.1:g.7902A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000266126.10:c.598-56A>G MANE Select ENSP00000266126.5:n.598-56A>G
ENST00000266126.9:c.598-56A>G ENSP00000266126.5:n.598-56A>G
ENST00000553401.5:c.571-31A>G ENSP00000451681.1:n.571-31A>G
ENST00000556028.5:c.598-87A>G ENSP00000452311.1:n.598-87A>G
NM_014239.3:c.598-56A>G NP_055054.1:n.598-56A>G
NM_014239.4:c.598-56A>G MANE Select NP_055054.1:n.598-56A>G