Canonical Allele Identifier: CA734706999
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1006560255
MyVariant Identifiers: chr1:g.29161426C>A (hg19) chr1:g.28834914C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834914C>A , CM000663.2:g.28834914C>A GRCh38
NC_000001.10:g.29161426C>A , CM000663.1:g.29161426C>A GRCh37
NC_000001.9:g.29034013C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22304C>A MANE Select ENSP00000234961.2:n.227+22304C>A
ENST00000234961.6:c.227+22304C>A ENSP00000234961.2:n.227+22304C>A
ENST00000621425.1:c.227+22304C>A ENSP00000477970.1:n.227+22304C>A
NM_000911.3:c.227+22304C>A NP_000902.3:n.227+22304C>A
NM_000911.4:c.227+22304C>A MANE Select NP_000902.3:n.227+22304C>A
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