Canonical Allele Identifier: CA1306207355

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944881T= , CM000664.2:g.168944881T=	GRCh38
NC_000002.11:g.169801391T= , CM000664.1:g.169801391T=	GRCh37
NC_000002.10:g.169509637T=	NCBI36
NG_007374.1:g.91443A=
NG_007374.2:g.91516A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.741A=	ENSP00000497165.1:p.Val247=
ENST00000650372.1:c.2424A= MANE Select	ENSP00000497931.1:p.Val808=
ENST00000263817.6:c.2424A=	ENSP00000263817.6:p.Val808=
ENST00000439188.1:c.1113A=	ENSP00000416058.1:n.1113A=
NM_003742.2:c.2424A=	NP_003733.2:p.Val808=
XM_006712817.2:c.2466A=	XP_006712880.1:p.Val822=
XM_011512077.1:c.2526A=	XP_011510379.1:p.Val842=
XM_011512078.1:c.2526A=	XP_011510380.1:p.Val842=
XM_011512079.1:c.2526A=	XP_011510381.1:p.Val842=
XM_011512080.1:c.2526A=	XP_011510382.1:p.Val842=
XM_011512081.1:c.750A=	XP_011510383.1:p.Val250=
NM_003742.4:c.2424A= MANE Select	NP_003733.2:p.Val808=
XM_006712817.3:c.2466A=	XP_006712880.1:p.Val822=
XM_011512077.2:c.2526A=	XP_011510379.1:p.Val842=
XM_011512078.2:c.2526A=	XP_011510380.1:p.Val842=
XM_011512080.2:c.2526A=	XP_011510382.1:p.Val842=
XM_011512081.2:c.750A=	XP_011510383.1:p.Val250=
XM_017005165.1:c.2526A=	XP_016860654.1:p.Val842=
XM_017005166.1:c.1755A=	XP_016860655.1:p.Val585=
XM_017005167.1:c.1209A=	XP_016860656.1:p.Val403=