Canonical Allele Identifier: CA20031397
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs888180751
gnomAD v3: 1-28835176-C-T
gnomAD v4: 1-28835176-C-T
MyVariant Identifiers: chr1:g.29161688C>T (hg19) chr1:g.28835176C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835176C>T , CM000663.2:g.28835176C>T GRCh38
NC_000001.10:g.29161688C>T , CM000663.1:g.29161688C>T GRCh37
NC_000001.9:g.29034275C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22566C>T MANE Select ENSP00000234961.2:n.227+22566C>T
ENST00000234961.6:c.227+22566C>T ENSP00000234961.2:n.227+22566C>T
ENST00000621425.1:c.227+22566C>T ENSP00000477970.1:n.227+22566C>T
NM_000911.3:c.227+22566C>T NP_000902.3:n.227+22566C>T
NM_000911.4:c.227+22566C>T MANE Select NP_000902.3:n.227+22566C>T
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