Canonical Allele Identifier: CA1306208100

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168932358A= , CM000664.2:g.168932358A=	GRCh38
NC_000002.11:g.169788868A= , CM000664.1:g.169788868A=	GRCh37
NC_000002.10:g.169497114A=	NCBI36
NG_007374.1:g.103966T=
NG_007374.2:g.104039T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.1530+19T=	ENSP00000497165.1:n.1530+19T=
ENST00000650372.1:c.3213+19T= MANE Select	ENSP00000497931.1:n.3213+19T=
ENST00000263817.6:c.3213+19T=	ENSP00000263817.6:n.3213+19T=
ENST00000439188.1:c.1902+19T=	ENSP00000416058.1:n.1902+19T=
NM_003742.2:c.3213+19T=	NP_003733.2:n.3213+19T=
XM_006712817.2:c.3255+19T=	XP_006712880.1:n.3255+19T=
XM_011512077.1:c.3315+19T=	XP_011510379.1:n.3315+19T=
XM_011512078.1:c.3315+19T=	XP_011510380.1:n.3315+19T=
XM_011512079.1:c.3315+19T=	XP_011510381.1:n.3315+19T=
XM_011512081.1:c.1539+19T=	XP_011510383.1:n.1539+19T=
NM_003742.4:c.3213+19T= MANE Select	NP_003733.2:n.3213+19T=
XM_006712817.3:c.3255+19T=	XP_006712880.1:n.3255+19T=
XM_011512077.2:c.3315+19T=	XP_011510379.1:n.3315+19T=
XM_011512078.2:c.3315+19T=	XP_011510380.1:n.3315+19T=
XM_011512081.2:c.1539+19T=	XP_011510383.1:n.1539+19T=
XM_017005165.1:c.3315+19T=	XP_016860654.1:n.3315+19T=
XM_017005166.1:c.2544+19T=	XP_016860655.1:n.2544+19T=
XM_017005167.1:c.1998+19T=	XP_016860656.1:n.1998+19T=