Canonical Allele Identifier: CA522066793
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1198187255
gnomAD v2: 1-29161697-G-GC
gnomAD v3: 1-28835185-G-GC
gnomAD v4: 1-28835185-G-GC
MyVariant Identifiers: chr1:g.29161697_29161698insC (hg19) chr1:g.28835185_28835186insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835190dup , CM000663.2:g.28835190dup GRCh38
NC_000001.10:g.29161702dup , CM000663.1:g.29161702dup GRCh37
NC_000001.9:g.29034289dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22580dup MANE Select ENSP00000234961.2:n.227+22580dup
ENST00000234961.6:c.227+22580dup ENSP00000234961.2:n.227+22580dup
ENST00000621425.1:c.227+22580dup ENSP00000477970.1:n.227+22580dup
NM_000911.3:c.227+22580dup NP_000902.3:n.227+22580dup
NM_000911.4:c.227+22580dup MANE Select NP_000902.3:n.227+22580dup
Search 100 bp 5'
Search 100 bp 3'