LDH info

Canonical Allele Identifier: CA150253489
Gene: OPRM1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3778150

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154062523T>C , CM000668.2:g.154062523T>C GRCh38
NC_000006.11:g.154383658T>C , CM000668.1:g.154383658T>C GRCh37
NC_000006.10:g.154425351T>C NCBI36
NG_021208.1:g.57023T>C
NG_021208.2:g.57023T>C

Transcript Alleles

HGVS Amino-acid change
NM_000914.4:c.290+22689T>C VV NP_000905.3:p.=
NM_001008503.2:c.290+22689T>C VV NP_001008503.2:p.=
NM_001008504.3:c.290+22689T>C VV NP_001008504.2:p.=
NM_001008505.2:c.290+22689T>C VV NP_001008505.2:p.=
NM_001145279.3:c.569+22689T>C VV NP_001138751.1:p.=
NM_001145280.3:c.-10-27303T>C VV NP_001138752.1:p.=
NM_001145281.2:c.48-27303T>C VV NP_001138753.1:p.=
NM_001145282.2:c.290+22689T>C VV NP_001138754.1:p.=
NM_001145283.2:c.290+22689T>C VV NP_001138755.1:p.=
NM_001145284.3:c.290+22689T>C VV NP_001138756.1:p.=
NM_001145285.2:c.290+22689T>C VV NP_001138757.1:p.=
NM_001145286.2:c.290+22689T>C VV NP_001138758.1:p.=
NM_001285522.1:c.290+22689T>C VV NP_001272451.1:p.=
NM_001285523.1:c.290+22689T>C VV NP_001272452.1:p.=
NM_001285524.1:c.569+22689T>C VV NP_001272453.1:p.=
NR_104348.1:n.424+22689T>C
NR_104349.1:n.424+22689T>C
NR_104350.1:n.424+22689T>C
NR_104351.1:n.424+22689T>C
XM_006715497.2:c.*5-10992T>C XP_006715560.1:p.=
XM_011535849.1:c.569+22689T>C XP_011534151.1:p.=
NM_001285523.2:c.290+22689T>C VV NP_001272452.1:p.=
XM_017010907.2:c.477-10992T>C XP_016866396.1:p.=
ENST00000229768.9:c.290+22689T>C ENSP00000229768.5:p.=
ENST00000330432.11:c.290+22689T>C ENSP00000328264.7:p.=
ENST00000337049.8:c.290+22689T>C ENSP00000338381.4:p.=
ENST00000360422.8:c.476+22689T>C ENSP00000353598.5:p.=
ENST00000414028.6:c.290+22689T>C ENSP00000399359.2:p.=
ENST00000419506.6:c.290+22689T>C ENSP00000403549.2:p.=
ENST00000428397.6:c.290+22689T>C ENSP00000411903.2:p.=
ENST00000434900.6:c.569+22689T>C ENSP00000394624.2:p.=
ENST00000435918.6:c.290+22689T>C ENSP00000413752.2:p.=
ENST00000452687.6:c.290+22689T>C ENSP00000410497.2:p.=
ENST00000518759.5:c.48-27303T>C ENSP00000430260.1:p.=
ENST00000519083.5:c.290+22689T>C ENSP00000431048.1:p.=
ENST00000520282.5:c.434+22689T>C ENSP00000430247.1:p.=
ENST00000520708.5:c.-10-27303T>C ENSP00000430876.1:p.=
ENST00000522739.5:c.290+22689T>C ENSP00000428018.1:p.=
ENST00000523520.1:n.594-10992T>C
ENST00000524150.2:c.290+22689T>C ENSP00000430575.1:p.=
ENST00000524163.5:c.290+22689T>C ENSP00000430097.1:p.=