Canonical Allele Identifier: CA263654934

Gene: EIF2B2

Linked Data

• dbSNP Id: rs771416034
• gnomAD v2: 14-75472513-A-T
• gnomAD v4: 14-75005810-A-T
• MyVariant Identifiers: chr14:g.75472513A>T (hg19) ; chr14:g.75005810A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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