Canonical Allele Identifier: CA2147299495
Gene: EIF2B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75006002G= , CM000676.2:g.75006002G= GRCh38
NC_000014.8:g.75472705G= , CM000676.1:g.75472705G= GRCh37
NC_000014.7:g.74542458G= NCBI36
NG_013333.1:g.8094G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266126.10:c.693+41G= MANE Select ENSP00000266126.5:n.693+41G=
ENST00000266126.9:c.693+41G= ENSP00000266126.5:n.693+41G=
ENST00000553401.5:c.691+41G= ENSP00000451681.1:n.691+41G=
ENST00000554748.2:c.57+41G= ENSP00000452582.2:n.57+41G=
ENST00000556028.5:c.*41+41G= ENSP00000452311.1:n.*41+41G=
NM_014239.3:c.693+41G= NP_055054.1:n.693+41G=
NM_014239.4:c.693+41G= MANE Select NP_055054.1:n.693+41G=
Search 100 bp 5'
Search 100 bp 3'