Canonical Allele Identifier: CA2068931444
Gene: EIF2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123630307G= , CM000674.2:g.123630307G= GRCh38
NC_000012.11:g.124114854G= , CM000674.1:g.124114854G= GRCh37
NC_000012.10:g.122680807G= NCBI36
NG_015862.1:g.8470C=

Transcript Alleles

HGVS Amino-acid change
ENST00000424014.7:c.253-22C= MANE Select ENSP00000416250.2:n.253-22C=
ENST00000424014.6:c.253-22C= ENSP00000416250.2:n.253-22C=
ENST00000452159.6:n.384-22C=
ENST00000534960.5:c.300-22C=
ENST00000537073.1:c.253-22C= ENSP00000444183.1:n.253-22C=
ENST00000539951.5:c.214-22C= ENSP00000438060.1:n.214-22C=
ENST00000543940.1:n.353-3C=
NM_001414.3:c.253-22C= NP_001405.1:n.253-22C=
NM_001414.4:c.253-22C= MANE Select NP_001405.1:n.253-22C=