Canonical Allele Identifier: CA20031337

Gene: OPRD1

Linked Data

• dbSNP Id: rs918771174
• MyVariant Identifiers: chr1:g.29161646A>G (hg19) ; chr1:g.28835134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.28835134A>G , CM000663.2:g.28835134A>G	GRCh38
NC_000001.10:g.29161646A>G , CM000663.1:g.29161646A>G	GRCh37
NC_000001.9:g.29034233A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000234961.7:c.227+22524A>G MANE Select	ENSP00000234961.2:n.227+22524A>G
ENST00000234961.6:c.227+22524A>G	ENSP00000234961.2:n.227+22524A>G
ENST00000621425.1:c.227+22524A>G	ENSP00000477970.1:n.227+22524A>G
NM_000911.3:c.227+22524A>G	NP_000902.3:n.227+22524A>G
NM_000911.4:c.227+22524A>G MANE Select	NP_000902.3:n.227+22524A>G