Canonical Allele Identifier: CA1161091782
Gene: OPRD1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834942T= , CM000663.2:g.28834942T= GRCh38
NC_000001.10:g.29161454T= , CM000663.1:g.29161454T= GRCh37
NC_000001.9:g.29034041T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22332T= MANE Select ENSP00000234961.2:n.227+22332T=
ENST00000234961.6:c.227+22332T= ENSP00000234961.2:n.227+22332T=
ENST00000621425.1:c.227+22332T= ENSP00000477970.1:n.227+22332T=
NM_000911.3:c.227+22332T= NP_000902.3:n.227+22332T=
NM_000911.4:c.227+22332T= MANE Select NP_000902.3:n.227+22332T=
Search 100 bp 5'
Search 100 bp 3'