Canonical Allele Identifier: CA10666101
Gene: OPRD1 HGNC NCBI
COSMIC:
COSN6452259 (not active)
MyVariant.info:
GRCh38 chr1:g.28848434A>C
GRCh37 chr1:g.29174946A>C
gnomAD v2:
1:29174946 A / C
gnomAD v3:
1:28848434 A / C
gnomAD v4:
chr1-28848434-A-C
Joint Max Group AF 0.84947185 (EAS)
Genomes Max Group AF 0.84947185 (EAS)
dbSNP:
529520
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28848434A>C , CM000663.2:g.28848434A>C GRCh38
NC_000001.10:g.29174946A>C , CM000663.1:g.29174946A>C GRCh37
NC_000001.9:g.29047533A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.228-10520A>C MANE Select ENSP00000234961.2:n.228-10520A>C
ENST00000234961.6:c.228-10520A>C ENSP00000234961.2:n.228-10520A>C
ENST00000621425.1:c.228-10520A>C ENSP00000477970.1:n.228-10520A>C
NM_000911.3:c.228-10520A>C NP_000902.3:n.228-10520A>C
NM_000911.4:c.228-10520A>C MANE Select NP_000902.3:n.228-10520A>C
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