Canonical Allele Identifier: CA1161091771
Gene: OPRD1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834929A= , CM000663.2:g.28834929A= GRCh38
NC_000001.10:g.29161441A= , CM000663.1:g.29161441A= GRCh37
NC_000001.9:g.29034028A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22319A= MANE Select ENSP00000234961.2:n.227+22319A=
ENST00000234961.6:c.227+22319A= ENSP00000234961.2:n.227+22319A=
ENST00000621425.1:c.227+22319A= ENSP00000477970.1:n.227+22319A=
NM_000911.3:c.227+22319A= NP_000902.3:n.227+22319A=
NM_000911.4:c.227+22319A= MANE Select NP_000902.3:n.227+22319A=
Search 100 bp 5'
Search 100 bp 3'