Canonical Allele Identifier: CA1306213476

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944629A= , CM000664.2:g.168944629A=	GRCh38
NC_000002.11:g.169801139A= , CM000664.1:g.169801139A=	GRCh37
NC_000002.10:g.169509385A=	NCBI36
NG_007374.1:g.91695T=
NG_007374.2:g.91768T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649448.1:c.903T=	ENSP00000497165.1:p.Ala301=
ENST00000650372.1:c.2586T= MANE Select	ENSP00000497931.1:p.Ala862=
ENST00000263817.6:c.2586T=	ENSP00000263817.6:p.Ala862=
ENST00000439188.1:c.1275T=	ENSP00000416058.1:n.1275T=
NM_003742.2:c.2586T=	NP_003733.2:p.Ala862=
XM_006712817.2:c.2628T=	XP_006712880.1:p.Ala876=
XM_011512077.1:c.2688T=	XP_011510379.1:p.Ala896=
XM_011512078.1:c.2688T=	XP_011510380.1:p.Ala896=
XM_011512079.1:c.2688T=	XP_011510381.1:p.Ala896=
XM_011512080.1:c.2688T=	XP_011510382.1:p.Ala896=
XM_011512081.1:c.912T=	XP_011510383.1:p.Ala304=
NM_003742.4:c.2586T= MANE Select	NP_003733.2:p.Ala862=
XM_006712817.3:c.2628T=	XP_006712880.1:p.Ala876=
XM_011512077.2:c.2688T=	XP_011510379.1:p.Ala896=
XM_011512078.2:c.2688T=	XP_011510380.1:p.Ala896=
XM_011512080.2:c.2688T=	XP_011510382.1:p.Ala896=
XM_011512081.2:c.912T=	XP_011510383.1:p.Ala304=
XM_017005165.1:c.2688T=	XP_016860654.1:p.Ala896=
XM_017005166.1:c.1917T=	XP_016860655.1:p.Ala639=
XM_017005167.1:c.1371T=	XP_016860656.1:p.Ala457=