Canonical Allele Identifier: CA1306205683

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168923386T= , CM000664.2:g.168923386T=	GRCh38
NC_000002.11:g.169779896T= , CM000664.1:g.169779896T=	GRCh37
NC_000002.10:g.169488142T=	NCBI36
NG_007374.1:g.112938A=
NG_007374.2:g.113011A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648875.1:c.226+1271A=
ENST00000649448.1:c.2579A=	ENSP00000497165.1:n.2579A=
ENST00000650372.1:c.*236A= MANE Select	ENSP00000497931.1:n.*236A=
ENST00000263817.6:c.*236A=	ENSP00000263817.6:n.*236A=
ENST00000439188.1:c.2819A=	ENSP00000416058.1:n.2819A=
NM_003742.2:c.*236A=	NP_003733.2:n.*236A=
XM_006712817.2:c.*236A=	XP_006712880.1:n.*236A=
XM_011512077.1:c.*236A=	XP_011510379.1:n.*236A=
XM_011512078.1:c.*190A=	XP_011510380.1:n.*190A=
XM_011512079.1:c.*236A=	XP_011510381.1:n.*236A=
XM_011512081.1:c.*236A=	XP_011510383.1:n.*236A=
NM_003742.4:c.*236A= MANE Select	NP_003733.2:n.*236A=
XM_006712817.3:c.*236A=	XP_006712880.1:n.*236A=
XM_011512077.2:c.*236A=	XP_011510379.1:n.*236A=
XM_011512078.2:c.*190A=	XP_011510380.1:n.*190A=
XM_011512081.2:c.*236A=	XP_011510383.1:n.*236A=
XM_017005165.1:c.3867+1271A=	XP_016860654.1:n.3867+1271A=
XM_017005166.1:c.*236A=	XP_016860655.1:n.*236A=
XM_017005167.1:c.*236A=	XP_016860656.1:n.*236A=