Canonical Allele Identifier: CA734706938
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1309002277
gnomAD v3: 1-28834651-A-G
gnomAD v4: 1-28834651-A-G
MyVariant Identifiers: chr1:g.29161163A>G (hg19) chr1:g.28834651A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834651A>G , CM000663.2:g.28834651A>G GRCh38
NC_000001.10:g.29161163A>G , CM000663.1:g.29161163A>G GRCh37
NC_000001.9:g.29033750A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22041A>G MANE Select ENSP00000234961.2:n.227+22041A>G
ENST00000234961.6:c.227+22041A>G ENSP00000234961.2:n.227+22041A>G
ENST00000621425.1:c.227+22041A>G ENSP00000477970.1:n.227+22041A>G
NM_000911.3:c.227+22041A>G NP_000902.3:n.227+22041A>G
NM_000911.4:c.227+22041A>G MANE Select NP_000902.3:n.227+22041A>G
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