Canonical Allele Identifier: CA1000026878
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs2088841729
gnomAD v3: 1-28835180-C-T
gnomAD v4: 1-28835180-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835180C>T , CM000663.2:g.28835180C>T GRCh38
NC_000001.10:g.29161692C>T , CM000663.1:g.29161692C>T GRCh37
NC_000001.9:g.29034279C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22570C>T MANE Select ENSP00000234961.2:n.227+22570C>T
ENST00000234961.6:c.227+22570C>T ENSP00000234961.2:n.227+22570C>T
ENST00000621425.1:c.227+22570C>T ENSP00000477970.1:n.227+22570C>T
NM_000911.3:c.227+22570C>T NP_000902.3:n.227+22570C>T
NM_000911.4:c.227+22570C>T MANE Select NP_000902.3:n.227+22570C>T
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