Canonical Allele Identifier: CA2068931471
Gene: EIF2B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123630328T= , CM000674.2:g.123630328T= GRCh38
NC_000012.11:g.124114875T= , CM000674.1:g.124114875T= GRCh37
NC_000012.10:g.122680828T= NCBI36
NG_015862.1:g.8449A=

Transcript Alleles

HGVS Amino-acid change
ENST00000424014.7:c.253-43A= MANE Select ENSP00000416250.2:n.253-43A=
ENST00000424014.6:c.253-43A= ENSP00000416250.2:n.253-43A=
ENST00000452159.6:n.384-43A=
ENST00000534960.5:c.300-43A=
ENST00000537073.1:c.253-43A= ENSP00000444183.1:n.253-43A=
ENST00000539951.5:c.214-43A= ENSP00000438060.1:n.214-43A=
ENST00000543940.1:n.353-24A=
NM_001414.3:c.253-43A= NP_001405.1:n.253-43A=
NM_001414.4:c.253-43A= MANE Select NP_001405.1:n.253-43A=
Search 100 bp 5'
Search 100 bp 3'