Canonical Allele Identifier: CA1360533946

Gene: ACKR2 KRBOX1 CYP8B1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42864624T= , CM000665.2:g.42864624T=	GRCh38
NC_000003.11:g.42906116T= , CM000665.1:g.42906116T=	GRCh37
NC_000003.10:g.42881120T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422265.6:c.122T= (ACKR2) MANE Select	ENSP00000416996.1:p.Val41=
ENST00000422265.5:c.122T= (ACKR2)	ENSP00000416996.1:p.Val41=
ENST00000426937.5:c.-163-44169T= (KRBOX1)	ENSP00000413859.1:n.-163-44169T=
ENST00000437102.1:c.1348-8153A= (CYP8B1)	ENSP00000404499.1:n.1348-8153A=
ENST00000442925.5:c.122T= (ACKR2)	ENSP00000396150.1:p.Val41=
ENST00000451200.6:n.168+44913T=
ENST00000460855.5:n.236T= (ACKR2)
ENST00000492609.1:c.122T= (ACKR2)	ENSP00000477475.1:p.Val41=
ENST00000493193.1:c.122T= (ACKR2)	ENSP00000476581.1:p.Val41=
ENST00000494619.1:c.122T= (ACKR2)	ENSP00000477157.1:p.Val41=
ENST00000497921.2:c.122T= (ACKR2)	ENSP00000476901.1:p.Val41=
ENST00000498111.5:n.311T= (ACKR2)
NM_001296.4:c.122T= (ACKR2)	NP_001287.2:p.Val41=
NM_001296.5:c.122T= (ACKR2) MANE Select	NP_001287.2:p.Val41=