Canonical Allele Identifier: CA734707024
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1018229885
MyVariant Identifiers: chr1:g.29161449G>C (hg19) chr1:g.28834937G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834937G>C , CM000663.2:g.28834937G>C GRCh38
NC_000001.10:g.29161449G>C , CM000663.1:g.29161449G>C GRCh37
NC_000001.9:g.29034036G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22327G>C MANE Select ENSP00000234961.2:n.227+22327G>C
ENST00000234961.6:c.227+22327G>C ENSP00000234961.2:n.227+22327G>C
ENST00000621425.1:c.227+22327G>C ENSP00000477970.1:n.227+22327G>C
NM_000911.3:c.227+22327G>C NP_000902.3:n.227+22327G>C
NM_000911.4:c.227+22327G>C MANE Select NP_000902.3:n.227+22327G>C
Search 100 bp 5'
Search 100 bp 3'