Canonical Allele Identifier: CA20031360
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs930129648
MyVariant Identifiers: chr1:g.29161677G>A (hg19) chr1:g.28835165G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835165G>A , CM000663.2:g.28835165G>A GRCh38
NC_000001.10:g.29161677G>A , CM000663.1:g.29161677G>A GRCh37
NC_000001.9:g.29034264G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22555G>A MANE Select ENSP00000234961.2:n.227+22555G>A
ENST00000234961.6:c.227+22555G>A ENSP00000234961.2:n.227+22555G>A
ENST00000621425.1:c.227+22555G>A ENSP00000477970.1:n.227+22555G>A
NM_000911.3:c.227+22555G>A NP_000902.3:n.227+22555G>A
NM_000911.4:c.227+22555G>A MANE Select NP_000902.3:n.227+22555G>A
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