Canonical Allele Identifier: CA522066770
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1448265300
gnomAD v2: 1-29161459-C-T
gnomAD v3: 1-28834947-C-T
gnomAD v4: 1-28834947-C-T
MyVariant Identifiers: chr1:g.29161459C>T (hg19) chr1:g.28834947C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834947C>T , CM000663.2:g.28834947C>T GRCh38
NC_000001.10:g.29161459C>T , CM000663.1:g.29161459C>T GRCh37
NC_000001.9:g.29034046C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22337C>T MANE Select ENSP00000234961.2:n.227+22337C>T
ENST00000234961.6:c.227+22337C>T ENSP00000234961.2:n.227+22337C>T
ENST00000621425.1:c.227+22337C>T ENSP00000477970.1:n.227+22337C>T
NM_000911.3:c.227+22337C>T NP_000902.3:n.227+22337C>T
NM_000911.4:c.227+22337C>T MANE Select NP_000902.3:n.227+22337C>T
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