Canonical Allele Identifier: CA522066781
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1332310780
gnomAD v2: 1-29161602-C-A
gnomAD v3: 1-28835090-C-A
gnomAD v4: 1-28835090-C-A
MyVariant Identifiers: chr1:g.29161602C>A (hg19) chr1:g.28835090C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28835090C>A , CM000663.2:g.28835090C>A GRCh38
NC_000001.10:g.29161602C>A , CM000663.1:g.29161602C>A GRCh37
NC_000001.9:g.29034189C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22480C>A MANE Select ENSP00000234961.2:n.227+22480C>A
ENST00000234961.6:c.227+22480C>A ENSP00000234961.2:n.227+22480C>A
ENST00000621425.1:c.227+22480C>A ENSP00000477970.1:n.227+22480C>A
NM_000911.3:c.227+22480C>A NP_000902.3:n.227+22480C>A
NM_000911.4:c.227+22480C>A MANE Select NP_000902.3:n.227+22480C>A
Search 100 bp 5'
Search 100 bp 3'