Canonical Allele Identifier: CA20031245
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs887085881
MyVariant Identifiers: chr1:g.29161421A>C (hg19) chr1:g.28834909A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834909A>C , CM000663.2:g.28834909A>C GRCh38
NC_000001.10:g.29161421A>C , CM000663.1:g.29161421A>C GRCh37
NC_000001.9:g.29034008A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22299A>C MANE Select ENSP00000234961.2:n.227+22299A>C
ENST00000234961.6:c.227+22299A>C ENSP00000234961.2:n.227+22299A>C
ENST00000621425.1:c.227+22299A>C ENSP00000477970.1:n.227+22299A>C
NM_000911.3:c.227+22299A>C NP_000902.3:n.227+22299A>C
NM_000911.4:c.227+22299A>C MANE Select NP_000902.3:n.227+22299A>C
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