Canonical Allele Identifier: CA599086960
Gene: NR1H3 HGNC NCBI

Linked Data

dbSNP Id: rs1242317771

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47259006G>C , CM000673.2:g.47259006G>C GRCh38
NC_000011.9:g.47280557G>C , CM000673.1:g.47280557G>C GRCh37
NC_000011.8:g.47237133G>C NCBI36
NG_030392.1:g.15707G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000441012.7:c.-37-174G>C MANE Select ENSP00000387946.2:n.-37-174G>C
ENST00000395397.7:c.-92-785G>C ENSP00000378793.3:n.-92-785G>C
ENST00000405576.5:c.-92-785G>C ENSP00000385073.1:n.-92-785G>C
ENST00000405853.7:c.-37-174G>C ENSP00000384745.3:n.-37-174G>C
ENST00000407404.5:c.-37-174G>C ENSP00000385801.1:n.-37-174G>C
ENST00000412937.5:c.-92-785G>C ENSP00000412636.1:n.-92-785G>C
ENST00000419652.5:c.-37-174G>C ENSP00000407716.1:n.-37-174G>C
ENST00000420369.5:c.-37-174G>C ENSP00000406692.1:n.-37-174G>C
ENST00000436029.5:c.-116-95G>C ENSP00000403696.1:n.-116-95G>C
ENST00000436778.5:c.-37-174G>C ENSP00000403798.1:n.-37-174G>C
ENST00000437276.1:c.-32-179G>C ENSP00000396132.1:n.-32-179G>C
ENST00000441012.6:c.-37-174G>C ENSP00000387946.2:n.-37-174G>C
ENST00000444396.5:c.-37-174G>C ENSP00000391005.1:n.-37-174G>C
ENST00000449369.5:c.-37-174G>C ENSP00000415591.1:n.-37-174G>C
ENST00000457932.5:c.-37-174G>C ENSP00000413095.1:n.-37-174G>C
ENST00000461778.5:n.214-95G>C
ENST00000467728.5:c.-211G>C ENSP00000420656.1:n.-211G>C
ENST00000476086.6:n.130-785G>C
ENST00000481020.5:n.77-785G>C
ENST00000481889.6:c.-92-785G>C ENSP00000433271.1:n.-92-785G>C
ENST00000487913.5:n.74-2235G>C
ENST00000495866.5:n.283-785G>C
ENST00000498548.1:n.127G>C
ENST00000525441.5:n.161-174G>C
ENST00000527464.5:n.283-785G>C
ENST00000529540.5:n.231-785G>C
ENST00000530310.1:n.61-174G>C
ENST00000531660.5:c.-92-785G>C ENSP00000434650.1:n.-92-785G>C
ENST00000532630.1:n.74-8907G>C
ENST00000616973.4:c.62-785G>C ENSP00000477707.1:n.62-785G>C
NM_001130101.2:c.-37-174G>C NP_001123573.1:n.-37-174G>C
NM_001130102.2:c.-92-785G>C NP_001123574.1:n.-92-785G>C
NM_001251934.1:c.62-785G>C NP_001238863.1:n.62-785G>C
NM_001251935.1:c.62-785G>C NP_001238864.1:n.62-785G>C
NM_005693.3:c.-37-174G>C NP_005684.2:n.-37-174G>C
XM_005252705.1:c.-37-174G>C XP_005252762.1:n.-37-174G>C
XM_005252706.1:c.-37-174G>C XP_005252763.1:n.-37-174G>C
XM_005252707.3:c.-116-95G>C XP_005252764.1:n.-116-95G>C
XM_005252709.1:c.-177-174G>C XP_005252766.1:n.-177-174G>C
XM_005252710.1:c.-177-174G>C XP_005252767.1:n.-177-174G>C
XM_005252713.2:c.-37-174G>C XP_005252770.1:n.-37-174G>C
XM_005252715.2:c.-37-174G>C XP_005252772.1:n.-37-174G>C
XM_005252716.2:c.-92-785G>C XP_005252773.1:n.-92-785G>C
XM_005252718.2:c.-92-785G>C XP_005252775.1:n.-92-785G>C
XM_006718112.1:c.-37-174G>C XP_006718175.1:n.-37-174G>C
XM_006718113.1:c.-37-174G>C XP_006718176.1:n.-37-174G>C
XM_006718114.2:c.-116-95G>C XP_006718177.1:n.-116-95G>C
XM_006718115.1:c.-177-174G>C XP_006718178.1:n.-177-174G>C
XM_006718116.1:c.-92-785G>C XP_006718179.1:n.-92-785G>C
XM_011519805.1:c.-37-174G>C XP_011518107.1:n.-37-174G>C
XM_011519806.1:c.-92-785G>C XP_011518108.1:n.-92-785G>C
XM_011519807.1:c.-92-785G>C XP_011518109.1:n.-92-785G>C
XM_011519808.1:c.-137-2235G>C XP_011518110.1:n.-137-2235G>C
NM_001363595.1:c.-92-785G>C NP_001350524.1:n.-92-785G>C
XM_005252713.3:c.-37-174G>C XP_005252770.1:n.-37-174G>C
XM_005252718.3:c.-92-785G>C XP_005252775.1:n.-92-785G>C
XM_011519805.2:c.-37-174G>C XP_011518107.1:n.-37-174G>C
XM_011519808.2:c.-137-2235G>C XP_011518110.1:n.-137-2235G>C
XM_017017056.1:c.-92-785G>C XP_016872545.1:n.-92-785G>C
XM_017017057.1:c.-92-785G>C XP_016872546.1:n.-92-785G>C
XM_024448284.1:c.-37-174G>C XP_024304052.1:n.-37-174G>C
XM_024448285.1:c.-37-174G>C XP_024304053.1:n.-37-174G>C
XM_024448286.1:c.-116-95G>C XP_024304054.1:n.-116-95G>C
XM_024448287.1:c.-37-174G>C XP_024304055.1:n.-37-174G>C
XM_024448288.1:c.-37-174G>C XP_024304056.1:n.-37-174G>C
XM_024448289.1:c.-92-785G>C XP_024304057.1:n.-92-785G>C
XM_024448290.1:c.-177-174G>C XP_024304058.1:n.-177-174G>C
XM_024448291.1:c.-177-174G>C XP_024304059.1:n.-177-174G>C
XM_024448292.1:c.-92-785G>C XP_024304060.1:n.-92-785G>C
XM_024448293.1:c.-177-174G>C XP_024304061.1:n.-177-174G>C
XM_024448294.1:c.-97-780G>C XP_024304062.1:n.-97-780G>C
XM_024448295.1:c.-92-785G>C XP_024304063.1:n.-92-785G>C
XM_024448296.1:c.-92-785G>C XP_024304064.1:n.-92-785G>C
XM_024448297.1:c.-37-174G>C XP_024304065.1:n.-37-174G>C
XM_024448298.1:c.-92-785G>C XP_024304066.1:n.-92-785G>C
XM_024448299.1:c.-92-785G>C XP_024304067.1:n.-92-785G>C
XM_024448300.1:c.-92-785G>C XP_024304068.1:n.-92-785G>C
XM_024448302.1:c.-137-2235G>C XP_024304070.1:n.-137-2235G>C
NM_005693.4:c.-37-174G>C MANE Select NP_005684.2:n.-37-174G>C
NM_001130101.3:c.-37-174G>C NP_001123573.1:n.-37-174G>C
NM_001130102.3:c.-92-785G>C NP_001123574.1:n.-92-785G>C
NM_001363595.2:c.-92-785G>C NP_001350524.1:n.-92-785G>C
NM_001251934.2:c.62-785G>C NP_001238863.1:n.62-785G>C
NM_001251935.2:c.62-785G>C NP_001238864.1:n.62-785G>C