Canonical Allele Identifier: CA20031148
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs750486105
gnomAD v3: 1-28834745-C-G
gnomAD v4: 1-28834745-C-G
MyVariant Identifiers: chr1:g.29161257C>G (hg19) chr1:g.28834745C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834745C>G , CM000663.2:g.28834745C>G GRCh38
NC_000001.10:g.29161257C>G , CM000663.1:g.29161257C>G GRCh37
NC_000001.9:g.29033844C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22135C>G MANE Select ENSP00000234961.2:n.227+22135C>G
ENST00000234961.6:c.227+22135C>G ENSP00000234961.2:n.227+22135C>G
ENST00000621425.1:c.227+22135C>G ENSP00000477970.1:n.227+22135C>G
NM_000911.3:c.227+22135C>G NP_000902.3:n.227+22135C>G
NM_000911.4:c.227+22135C>G MANE Select NP_000902.3:n.227+22135C>G
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