Canonical Allele Identifier: CA522066768

Gene: OPRD1

Linked Data

• dbSNP Id: rs1207780574
• gnomAD v2: 1-29161443-T-C
• gnomAD v3: 1-28834931-T-C
• gnomAD v4: 1-28834931-T-C
• MyVariant Identifiers: chr1:g.29161443T>C (hg19) ; chr1:g.28834931T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.28834931T>C , CM000663.2:g.28834931T>C	GRCh38
NC_000001.10:g.29161443T>C , CM000663.1:g.29161443T>C	GRCh37
NC_000001.9:g.29034030T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234961.7:c.227+22321T>C MANE Select	ENSP00000234961.2:n.227+22321T>C
ENST00000234961.6:c.227+22321T>C	ENSP00000234961.2:n.227+22321T>C
ENST00000621425.1:c.227+22321T>C	ENSP00000477970.1:n.227+22321T>C
NM_000911.3:c.227+22321T>C	NP_000902.3:n.227+22321T>C
NM_000911.4:c.227+22321T>C MANE Select	NP_000902.3:n.227+22321T>C