Canonical Allele Identifier: CA10864157
Gene: OPRD1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2236857

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835097T>C , CM000663.2:g.28835097T>C GRCh38
NC_000001.10:g.29161609T>C , CM000663.1:g.29161609T>C GRCh37
NC_000001.9:g.29034196T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000911.3:c.227+22487T>C VV NP_000902.3:p.=
NM_000911.4:c.227+22487T>C VV MANE Preferred
ENST00000234961.6:c.227+22487T>C ENSP00000234961.2:p.=
ENST00000621425.1:c.227+22487T>C ENSP00000477970.1:p.=