Canonical Allele Identifier: CA1000026780
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs2088836537
gnomAD v3: 1-28834774-A-T
gnomAD v4: 1-28834774-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834774A>T , CM000663.2:g.28834774A>T GRCh38
NC_000001.10:g.29161286A>T , CM000663.1:g.29161286A>T GRCh37
NC_000001.9:g.29033873A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22164A>T MANE Select ENSP00000234961.2:n.227+22164A>T
ENST00000234961.6:c.227+22164A>T ENSP00000234961.2:n.227+22164A>T
ENST00000621425.1:c.227+22164A>T ENSP00000477970.1:n.227+22164A>T
NM_000911.3:c.227+22164A>T NP_000902.3:n.227+22164A>T
NM_000911.4:c.227+22164A>T MANE Select NP_000902.3:n.227+22164A>T
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