Canonical Allele Identifier: CA452973447
Gene: OPRM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.154360436G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039301G>A , CM000668.2:g.154039301G>A GRCh38
NC_000006.11:g.154360436G>A , CM000668.1:g.154360436G>A GRCh37
NC_000006.10:g.154402129G>A NCBI36
NG_021208.1:g.33801G>A
NG_021208.2:g.33801G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.-244G>A MANE Select ENSP00000328264.7:n.-244G>A
ENST00000360422.8:c.-58G>A ENSP00000353598.5:n.-58G>A
ENST00000434900.6:c.141G>A ENSP00000394624.2:p.Gly47=
ENST00000518759.5:c.47+28742G>A ENSP00000430260.1:n.47+28742G>A
ENST00000520282.5:c.11-110G>A ENSP00000430247.1:n.11-110G>A
ENST00000520708.5:c.-11+28283G>A ENSP00000430876.1:n.-11+28283G>A
NM_000914.4:c.-244G>A NP_000905.3:n.-244G>A
NM_001008504.3:c.-244G>A NP_001008504.2:n.-244G>A
NM_001145279.3:c.141G>A NP_001138751.1:p.Gly47=
NM_001145280.3:c.-11+28283G>A NP_001138752.1:n.-11+28283G>A
NM_001145281.2:c.47+28742G>A NP_001138753.1:n.47+28742G>A
NM_001285522.1:c.-244G>A NP_001272451.1:n.-244G>A
NM_001285523.1:c.-244G>A NP_001272452.1:n.-244G>A
NM_001285524.1:c.141G>A NP_001272453.1:p.Gly47=
XM_006715497.2:c.-58G>A XP_006715560.1:n.-58G>A
XM_011535849.1:c.141G>A XP_011534151.1:p.Gly47=
NM_001285523.2:c.-244G>A NP_001272452.1:n.-244G>A
XM_017010907.2:c.-58G>A XP_016866396.1:n.-58G>A
NM_000914.5:c.-244G>A MANE Select NP_000905.3:n.-244G>A
NM_001008503.3:c.-244G>A NP_001008503.2:n.-244G>A
NM_001008504.4:c.-244G>A NP_001008504.2:n.-244G>A
NM_001145279.4:c.141G>A NP_001138751.1:p.Gly47=
NM_001145280.4:c.-11+28283G>A NP_001138752.1:n.-11+28283G>A
NM_001145281.3:c.47+28742G>A NP_001138753.1:n.47+28742G>A
NM_001145285.3:c.-244G>A NP_001138757.1:n.-244G>A
NM_001145286.3:c.-244G>A NP_001138758.1:n.-244G>A
NM_001285523.3:c.-244G>A NP_001272452.1:n.-244G>A