Canonical Allele Identifier: CA10666104
Gene: OPRD1 HGNC NCBI
COSMIC:
COSN6452261 (not active)
MyVariant.info:
GRCh38 chr1:g.28848861A>G
GRCh37 chr1:g.29175373A>G
gnomAD v2:
1:29175373 A / G
gnomAD v3:
1:28848861 A / G
gnomAD v4:
chr1-28848861-A-G
Joint Max Group AF 0.89320373 (EAS)
Genomes Max Group AF 0.89320373 (EAS)
dbSNP:
581111
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28848861A>G , CM000663.2:g.28848861A>G GRCh38
NC_000001.10:g.29175373A>G , CM000663.1:g.29175373A>G GRCh37
NC_000001.9:g.29047960A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.228-10093A>G MANE Select ENSP00000234961.2:n.228-10093A>G
ENST00000234961.6:c.228-10093A>G ENSP00000234961.2:n.228-10093A>G
ENST00000621425.1:c.228-10093A>G ENSP00000477970.1:n.228-10093A>G
NM_000911.3:c.228-10093A>G NP_000902.3:n.228-10093A>G
NM_000911.4:c.228-10093A>G MANE Select NP_000902.3:n.228-10093A>G
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