Canonical Allele Identifier: CA1161091956
Gene: OPRD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835178T= , CM000663.2:g.28835178T= GRCh38
NC_000001.10:g.29161690T= , CM000663.1:g.29161690T= GRCh37
NC_000001.9:g.29034277T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22568T= MANE Select ENSP00000234961.2:n.227+22568T=
ENST00000234961.6:c.227+22568T= ENSP00000234961.2:n.227+22568T=
ENST00000621425.1:c.227+22568T= ENSP00000477970.1:n.227+22568T=
NM_000911.3:c.227+22568T= NP_000902.3:n.227+22568T=
NM_000911.4:c.227+22568T= MANE Select NP_000902.3:n.227+22568T=
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