Canonical Allele Identifier: CA1723579235

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87452954G= , CM000669.2:g.87452954G=	GRCh38
NC_000007.13:g.87082270G= , CM000669.1:g.87082270G=	GRCh37
NC_000007.12:g.86920206G=	NCBI36
NG_007118.1:g.32479C=
NG_007118.2:g.32479C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.526C=	ENSP00000352135.3:p.Arg176=
ENST00000643670.1:c.469C=	ENSP00000496629.1:p.Arg157=
ENST00000644106.1:c.526C=	ENSP00000493477.1:p.Arg176=
ENST00000649586.2:c.526C= MANE Select	ENSP00000496956.2:p.Arg176=
ENST00000265723.8:c.526C=	ENSP00000265723.4:p.Arg176=
ENST00000358400.7:c.526C=	ENSP00000351172.3:p.Arg176=
ENST00000359206.7:c.526C=	ENSP00000352135.3:p.Arg176=
ENST00000453593.5:c.526C=	ENSP00000392983.1:p.Arg176=
ENST00000473795.1:n.533C=
NM_000443.3:c.526C=	NP_000434.1:p.Arg176=
NM_018849.2:c.526C=	NP_061337.1:p.Arg176=
NM_018850.2:c.526C=	NP_061338.1:p.Arg176=
XM_011516308.1:c.526C=	XP_011514610.1:p.Arg176=
XM_011516309.1:c.526C=	XP_011514611.1:p.Arg176=
XM_011516310.1:c.526C=	XP_011514612.1:p.Arg176=
XM_011516311.1:c.526C=	XP_011514613.1:p.Arg176=
XM_011516312.1:c.526C=	XP_011514614.1:p.Arg176=
XM_011516313.1:c.526C=	XP_011514615.1:p.Arg176=
XM_011516314.1:c.547C=	XP_011514616.1:p.Arg183=
XM_011516315.1:c.-58C=	XP_011514617.1:n.-58C=
XR_927478.1:n.622C=
XM_011516308.3:c.796C=	XP_011514610.3:p.Arg266=
XM_011516309.3:c.796C=	XP_011514611.3:p.Arg266=
XM_011516310.3:c.796C=	XP_011514612.3:p.Arg266=
XM_011516311.3:c.796C=	XP_011514613.3:p.Arg266=
XM_011516312.3:c.796C=	XP_011514614.3:p.Arg266=
XM_011516313.3:c.796C=	XP_011514615.2:p.Arg266=
XM_011516315.3:c.-58C=	XP_011514617.2:n.-58C=
XM_017012323.2:c.526C=	XP_016867812.1:p.Arg176=
XR_001744809.2:n.1297C=
XR_001744810.2:n.1292C=
NM_000443.4:c.526C= MANE Select	NP_000434.1:p.Arg176=
NM_018849.3:c.526C=	NP_061337.1:p.Arg176=
NM_018850.3:c.526C=	NP_061338.1:p.Arg176=