Canonical Allele Identifier: CA1969297130
Gene: NR1H3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47268596G= , CM000673.2:g.47268596G= GRCh38
NC_000011.9:g.47290147G= , CM000673.1:g.47290147G= GRCh37
NC_000011.8:g.47246723G= NCBI36
NG_029462.1:g.4221G=
NG_030392.1:g.25297G=

Transcript Alleles

HGVS Amino-acid Change
NM_005693.4:c.1244G= MANE Select NP_005684.2:p.Arg415=
ENST00000441012.7:c.1244G= MANE Select ENSP00000387946.2:p.Arg415=
NM_001130101.2:c.1064G= NP_001123573.1:p.Arg355=
NM_001130101.3:c.1064G= NP_001123573.1:p.Arg355=
NM_001130102.2:c.1109G= NP_001123574.1:p.Arg370=
NM_001130102.3:c.1109G= NP_001123574.1:p.Arg370=
NM_001251934.1:c.1262G= NP_001238863.1:p.Arg421=
NM_001251934.2:c.1262G= NP_001238863.1:p.Arg421=
NM_001251935.1:c.1262G= NP_001238864.1:p.Arg421=
NM_001251935.2:c.1262G= NP_001238864.1:p.Arg421=
NM_001363595.1:c.929G= NP_001350524.1:p.Arg310=
NM_001363595.2:c.929G= NP_001350524.1:p.Arg310=
NM_005693.3:c.1244G= NP_005684.2:p.Arg415=
ENST00000395397.7:c.1109G= ENSP00000378793.3:p.Arg370=
ENST00000405576.5:c.929G= ENSP00000385073.1:p.Arg310=
ENST00000405853.7:c.1064G= ENSP00000384745.3:p.Arg355=
ENST00000407404.5:c.1064G= ENSP00000385801.1:p.Arg355=
ENST00000441012.6:c.1244G= ENSP00000387946.2:p.Arg415=
ENST00000462051.5:n.458G=
ENST00000467728.5:c.1244G= ENSP00000420656.1:p.Arg415=
ENST00000481020.5:n.1469G=
ENST00000481889.6:c.1301G= ENSP00000433271.1:p.Arg434=
ENST00000494018.1:n.262G=
ENST00000527949.1:c.791G= ENSP00000432073.1:p.Arg264=
ENST00000529540.5:n.1431G=
ENST00000532630.1:n.329G=
ENST00000616973.4:c.1262G= ENSP00000477707.1:p.Arg421=
XM_005252705.1:c.1244G= XP_005252762.1:p.Arg415=
XM_005252706.1:c.1244G= XP_005252763.1:p.Arg415=
XM_005252707.3:c.1244G= XP_005252764.1:p.Arg415=
XM_005252709.1:c.1109G= XP_005252766.1:p.Arg370=
XM_005252710.1:c.1109G= XP_005252767.1:p.Arg370=
XM_005252713.2:c.1064G= XP_005252770.1:p.Arg355=
XM_005252713.3:c.1064G= XP_005252770.1:p.Arg355=
XM_005252715.2:c.977G= XP_005252772.1:p.Arg326=
XM_005252716.2:c.842G= XP_005252773.1:p.Arg281=
XM_005252718.2:c.662G= XP_005252775.1:p.Arg221=
XM_005252718.3:c.662G= XP_005252775.1:p.Arg221=
XM_006718112.1:c.1244G= XP_006718175.1:p.Arg415=
XM_006718113.1:c.1244G= XP_006718176.1:p.Arg415=
XM_006718114.2:c.1244G= XP_006718177.1:p.Arg415=
XM_006718115.1:c.1109G= XP_006718178.1:p.Arg370=
XM_006718116.1:c.1109G= XP_006718179.1:p.Arg370=
XM_011519805.1:c.1244G= XP_011518107.1:p.Arg415=
XM_011519805.2:c.1244G= XP_011518107.1:p.Arg415=
XM_011519806.1:c.929G= XP_011518108.1:p.Arg310=
XM_011519807.1:c.842G= XP_011518109.1:p.Arg281=
XM_011519808.1:c.608G= XP_011518110.1:p.Arg203=
XM_011519808.2:c.608G= XP_011518110.1:p.Arg203=
XM_024448284.1:c.1436G= XP_024304052.1:p.Arg479=
XM_024448285.1:c.1436G= XP_024304053.1:p.Arg479=
XM_024448286.1:c.1436G= XP_024304054.1:p.Arg479=
XM_024448287.1:c.1436G= XP_024304055.1:p.Arg479=
XM_024448288.1:c.1436G= XP_024304056.1:p.Arg479=
XM_024448289.1:c.1109G= XP_024304057.1:p.Arg370=
XM_024448290.1:c.1301G= XP_024304058.1:p.Arg434=
XM_024448291.1:c.1301G= XP_024304059.1:p.Arg434=
XM_024448292.1:c.1301G= XP_024304060.1:p.Arg434=
XM_024448293.1:c.1301G= XP_024304061.1:p.Arg434=
XM_024448294.1:c.1301G= XP_024304062.1:p.Arg434=
XM_024448295.1:c.1301G= XP_024304063.1:p.Arg434=
XM_024448296.1:c.1034G= XP_024304064.1:p.Arg345=
XM_024448297.1:c.1169G= XP_024304065.1:p.Arg390=
XM_024448298.1:c.1109G= XP_024304066.1:p.Arg370=
XM_024448299.1:c.1034G= XP_024304067.1:p.Arg345=
XM_024448300.1:c.1301G= XP_024304068.1:p.Arg434=
XM_024448302.1:c.800G= XP_024304070.1:p.Arg267=