Canonical Allele Identifier: CA522066763

Gene: OPRD1

Linked Data

• dbSNP Id: rs1317652065
• gnomAD v2: 1-29161318-C-T
• gnomAD v3: 1-28834806-C-T
• gnomAD v4: 1-28834806-C-T
• MyVariant Identifiers: chr1:g.29161318C>T (hg19) ; chr1:g.28834806C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.28834806C>T , CM000663.2:g.28834806C>T	GRCh38
NC_000001.10:g.29161318C>T , CM000663.1:g.29161318C>T	GRCh37
NC_000001.9:g.29033905C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234961.7:c.227+22196C>T MANE Select	ENSP00000234961.2:n.227+22196C>T
ENST00000234961.6:c.227+22196C>T	ENSP00000234961.2:n.227+22196C>T
ENST00000621425.1:c.227+22196C>T	ENSP00000477970.1:n.227+22196C>T
NM_000911.3:c.227+22196C>T	NP_000902.3:n.227+22196C>T
NM_000911.4:c.227+22196C>T MANE Select	NP_000902.3:n.227+22196C>T