Canonical Allele Identifier: CA452973608
Gene: OPRM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.154360613T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039478T>C , CM000668.2:g.154039478T>C GRCh38
NC_000006.11:g.154360613T>C , CM000668.1:g.154360613T>C GRCh37
NC_000006.10:g.154402306T>C NCBI36
NG_021208.1:g.33978T>C
NG_021208.2:g.33978T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000330432.12:c.-67T>C MANE Select ENSP00000328264.7:n.-67T>C
ENST00000330432.11:c.-67T>C ENSP00000328264.7:n.-67T>C
ENST00000360422.8:c.120T>C ENSP00000353598.5:p.Leu40=
ENST00000428397.6:c.-67T>C ENSP00000411903.2:n.-67T>C
ENST00000434900.6:c.213T>C ENSP00000394624.2:p.Leu71=
ENST00000452687.6:c.-67T>C ENSP00000410497.2:n.-67T>C
ENST00000518759.5:c.47+28919T>C ENSP00000430260.1:n.47+28919T>C
ENST00000520282.5:c.78T>C ENSP00000430247.1:p.Leu26=
ENST00000520708.5:c.-11+28460T>C ENSP00000430876.1:n.-11+28460T>C
ENST00000522739.5:c.-67T>C ENSP00000428018.1:n.-67T>C
ENST00000523520.1:n.115T>C
NM_000914.4:c.-67T>C NP_000905.3:n.-67T>C
NM_001008503.2:c.-67T>C NP_001008503.2:n.-67T>C
NM_001008504.3:c.-67T>C NP_001008504.2:n.-67T>C
NM_001008505.2:c.-67T>C NP_001008505.2:n.-67T>C
NM_001145279.3:c.213T>C NP_001138751.1:p.Leu71=
NM_001145280.3:c.-11+28460T>C NP_001138752.1:n.-11+28460T>C
NM_001145281.2:c.47+28919T>C NP_001138753.1:n.47+28919T>C
NM_001145282.2:c.-67T>C NP_001138754.1:n.-67T>C
NM_001145283.2:c.-67T>C NP_001138755.1:n.-67T>C
NM_001145284.3:c.-67T>C NP_001138756.1:n.-67T>C
NM_001145285.2:c.-67T>C NP_001138757.1:n.-67T>C
NM_001145286.2:c.-67T>C NP_001138758.1:n.-67T>C
NM_001285522.1:c.-67T>C NP_001272451.1:n.-67T>C
NM_001285523.1:c.-67T>C NP_001272452.1:n.-67T>C
NM_001285524.1:c.213T>C NP_001272453.1:p.Leu71=
NR_104348.1:n.68T>C
NR_104349.1:n.68T>C
NR_104350.1:n.68T>C
NR_104351.1:n.68T>C
XM_006715497.2:c.120T>C XP_006715560.1:p.Leu40=
XM_011535849.1:c.213T>C XP_011534151.1:p.Leu71=
NM_001285523.2:c.-67T>C NP_001272452.1:n.-67T>C
XM_017010907.2:c.120T>C XP_016866396.1:p.Leu40=
NM_000914.5:c.-67T>C MANE Select NP_000905.3:n.-67T>C
NM_001008503.3:c.-67T>C NP_001008503.2:n.-67T>C
NM_001008504.4:c.-67T>C NP_001008504.2:n.-67T>C
NM_001145279.4:c.213T>C NP_001138751.1:p.Leu71=
NM_001145280.4:c.-11+28460T>C NP_001138752.1:n.-11+28460T>C
NM_001145281.3:c.47+28919T>C NP_001138753.1:n.47+28919T>C
NM_001145285.3:c.-67T>C NP_001138757.1:n.-67T>C
NM_001145286.3:c.-67T>C NP_001138758.1:n.-67T>C
NM_001285523.3:c.-67T>C NP_001272452.1:n.-67T>C