Canonical Allele Identifier: CA10720200
Gene: OPRD1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.28863878T>A
GRCh37 chr1:g.29190390T>A
gnomAD v2:
1:29190390 T / A
gnomAD v3:
1:28863878 T / A
gnomAD v4:
chr1-28863878-T-A
Joint Max Group AF 0.88765777 (EAS)
Genomes Max Group AF 0.88761904 (EAS)
Exomes Max Group AF 0.51467155 (NFE)
dbSNP:
204076
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28863878T>A , CM000663.2:g.28863878T>A GRCh38
NC_000001.10:g.29190390T>A , CM000663.1:g.29190390T>A GRCh37
NC_000001.9:g.29062977T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.*595T>A MANE Select ENSP00000234961.2:n.*595T>A
ENST00000234961.6:c.*595T>A ENSP00000234961.2:n.*595T>A
NM_000911.4:c.*595T>A MANE Select NP_000902.3:n.*595T>A
Search 100 bp 5'
Search 100 bp 3'