Canonical Allele Identifier: CA1360537362

Gene: CYP8B1 KRBOX1 ACKR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42872520T= , CM000665.2:g.42872520T=	GRCh38
NC_000003.11:g.42914012T= , CM000665.1:g.42914012T=	GRCh37
NC_000003.10:g.42889016T=	NCBI36
NG_007970.1:g.8622A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316161.6:c.*1791A= (CYP8B1) MANE Select	ENSP00000318867.4:n.*1791A=
ENST00000316161.5:c.*1791A= (CYP8B1)	ENSP00000318867.4:n.*1791A=
ENST00000426937.5:c.-163-36273T= (KRBOX1)	ENSP00000413859.1:n.-163-36273T=
ENST00000437102.1:c.1347+1950A= (CYP8B1)	ENSP00000404499.1:n.1347+1950A=
ENST00000451200.6:n.168+52809T=
ENST00000460855.5:n.471+7661T= (ACKR2)
ENST00000498111.5:n.546+7661T= (ACKR2)
NM_004391.2:c.*1791A= (CYP8B1)	NP_004382.2:n.*1791A=
NM_004391.3:c.*1791A= (CYP8B1) MANE Select	NP_004382.2:n.*1791A=