Canonical Allele Identifier: CA1161091772
Gene: OPRD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834931T= , CM000663.2:g.28834931T= GRCh38
NC_000001.10:g.29161443T= , CM000663.1:g.29161443T= GRCh37
NC_000001.9:g.29034030T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22321T= MANE Select ENSP00000234961.2:n.227+22321T=
ENST00000234961.6:c.227+22321T= ENSP00000234961.2:n.227+22321T=
ENST00000621425.1:c.227+22321T= ENSP00000477970.1:n.227+22321T=
NM_000911.3:c.227+22321T= NP_000902.3:n.227+22321T=
NM_000911.4:c.227+22321T= MANE Select NP_000902.3:n.227+22321T=
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