Canonical Allele Identifier: CA2340868647

Gene: NR1H2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50377484T>G , CM000681.2:g.50377484T>G	GRCh38
NC_000019.9:g.50880741T>G , CM000681.1:g.50880741T>G	GRCh37
NC_000019.8:g.55572553T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253727.10:c.-19-103T>G MANE Select	ENSP00000253727.4:n.-19-103T>G
ENST00000652203.1:c.-19-103T>G	ENSP00000499121.1:n.-19-103T>G
ENST00000253727.9:c.-19-103T>G	ENSP00000253727.4:n.-19-103T>G
ENST00000411902.6:c.-19-103T>G	ENSP00000396151.2:n.-19-103T>G
ENST00000593532.5:c.-19-103T>G	ENSP00000472271.1:n.-19-103T>G
ENST00000593926.5:c.-19-103T>G	ENSP00000471194.1:n.-19-103T>G
ENST00000595730.5:n.229-103T>G
ENST00000597130.5:c.-53-69T>G	ENSP00000472138.1:n.-53-69T>G
ENST00000597157.1:c.-122T>G	ENSP00000469778.1:n.-122T>G
ENST00000597790.5:c.-19-103T>G	ENSP00000470518.1:n.-19-103T>G
ENST00000598168.5:c.-19-103T>G	ENSP00000471294.1:n.-19-103T>G
ENST00000599105.5:c.-19-103T>G	ENSP00000472526.1:n.-19-103T>G
ENST00000600355.5:c.-19-103T>G	ENSP00000473099.1:n.-19-103T>G
NM_001256647.1:c.-19-103T>G	NP_001243576.1:n.-19-103T>G
NM_007121.5:c.-19-103T>G	NP_009052.3:n.-19-103T>G
NM_001256647.2:c.-19-103T>G	NP_001243576.2:n.-19-103T>G
NM_007121.6:c.-19-103T>G	NP_009052.4:n.-19-103T>G
NM_007121.7:c.-19-103T>G MANE Select	NP_009052.4:n.-19-103T>G
NM_001256647.3:c.-19-103T>G	NP_001243576.2:n.-19-103T>G