Canonical Allele Identifier: CA20031298
Gene: OPRD1 HGNC NCBI

Linked Data

dbSNP Id: rs998484601
gnomAD v3: 1-28834967-T-G
gnomAD v4: 1-28834967-T-G
MyVariant Identifiers: chr1:g.29161479T>G (hg19) chr1:g.28834967T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834967T>G , CM000663.2:g.28834967T>G GRCh38
NC_000001.10:g.29161479T>G , CM000663.1:g.29161479T>G GRCh37
NC_000001.9:g.29034066T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234961.7:c.227+22357T>G MANE Select ENSP00000234961.2:n.227+22357T>G
ENST00000234961.6:c.227+22357T>G ENSP00000234961.2:n.227+22357T>G
ENST00000621425.1:c.227+22357T>G ENSP00000477970.1:n.227+22357T>G
NM_000911.3:c.227+22357T>G NP_000902.3:n.227+22357T>G
NM_000911.4:c.227+22357T>G MANE Select NP_000902.3:n.227+22357T>G
Search 100 bp 5'
Search 100 bp 3'