Canonical Allele Identifier: CA1161091722
Gene: OPRD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834826A= , CM000663.2:g.28834826A= GRCh38
NC_000001.10:g.29161338A= , CM000663.1:g.29161338A= GRCh37
NC_000001.9:g.29033925A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22216A= MANE Select ENSP00000234961.2:n.227+22216A=
ENST00000234961.6:c.227+22216A= ENSP00000234961.2:n.227+22216A=
ENST00000621425.1:c.227+22216A= ENSP00000477970.1:n.227+22216A=
NM_000911.3:c.227+22216A= NP_000902.3:n.227+22216A=
NM_000911.4:c.227+22216A= MANE Select NP_000902.3:n.227+22216A=