Canonical Allele Identifier: CA1306224836

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168970131G= , CM000664.2:g.168970131G=	GRCh38
NC_000002.11:g.169826641G= , CM000664.1:g.169826641G=	GRCh37
NC_000002.10:g.169534887G=	NCBI36
NG_007374.1:g.66193C=
NG_007374.2:g.66266C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.40C=	ENSP00000497165.1:p.Arg14=
ENST00000650372.1:c.1723C= MANE Select	ENSP00000497931.1:p.Arg575=
ENST00000263817.6:c.1723C=	ENSP00000263817.6:p.Arg575=
ENST00000439188.1:c.412C=	ENSP00000416058.1:n.412C=
ENST00000478354.1:n.461C=
NM_003742.2:c.1723C=	NP_003733.2:p.Arg575=
XM_006712817.2:c.1765C=	XP_006712880.1:p.Arg589=
XM_011512077.1:c.1825C=	XP_011510379.1:p.Arg609=
XM_011512078.1:c.1825C=	XP_011510380.1:p.Arg609=
XM_011512079.1:c.1825C=	XP_011510381.1:p.Arg609=
XM_011512080.1:c.1825C=	XP_011510382.1:p.Arg609=
XM_011512081.1:c.49C=	XP_011510383.1:p.Arg17=
NM_003742.4:c.1723C= MANE Select	NP_003733.2:p.Arg575=
XM_006712817.3:c.1765C=	XP_006712880.1:p.Arg589=
XM_011512077.2:c.1825C=	XP_011510379.1:p.Arg609=
XM_011512078.2:c.1825C=	XP_011510380.1:p.Arg609=
XM_011512080.2:c.1825C=	XP_011510382.1:p.Arg609=
XM_011512081.2:c.49C=	XP_011510383.1:p.Arg17=
XM_017005165.1:c.1825C=	XP_016860654.1:p.Arg609=
XM_017005166.1:c.1054C=	XP_016860655.1:p.Arg352=
XM_017005167.1:c.508C=	XP_016860656.1:p.Arg170=