Canonical Allele Identifier: CA1306201726

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168927847A= , CM000664.2:g.168927847A=	GRCh38
NC_000002.11:g.169784357A= , CM000664.1:g.169784357A=	GRCh37
NC_000002.10:g.169492603A=	NCBI36
NG_007374.1:g.108477T=
NG_007374.2:g.108550T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.1789-485T=	ENSP00000497165.1:n.1789-485T=
ENST00000650372.1:c.3412-485T= MANE Select	ENSP00000497931.1:n.3412-485T=
ENST00000263817.6:c.3412-485T=	ENSP00000263817.6:n.3412-485T=
ENST00000439188.1:c.2101-557T=	ENSP00000416058.1:n.2101-557T=
NM_003742.2:c.3412-485T=	NP_003733.2:n.3412-485T=
XM_006712817.2:c.3454-485T=	XP_006712880.1:n.3454-485T=
XM_011512077.1:c.3514-485T=	XP_011510379.1:n.3514-485T=
XM_011512078.1:c.3514-485T=	XP_011510380.1:n.3514-485T=
XM_011512079.1:c.3514-485T=	XP_011510381.1:n.3514-485T=
XM_011512081.1:c.1738-485T=	XP_011510383.1:n.1738-485T=
NM_003742.4:c.3412-485T= MANE Select	NP_003733.2:n.3412-485T=
XM_006712817.3:c.3454-485T=	XP_006712880.1:n.3454-485T=
XM_011512077.2:c.3514-485T=	XP_011510379.1:n.3514-485T=
XM_011512078.2:c.3514-485T=	XP_011510380.1:n.3514-485T=
XM_011512081.2:c.1738-485T=	XP_011510383.1:n.1738-485T=
XM_017005165.1:c.3514-485T=	XP_016860654.1:n.3514-485T=
XM_017005166.1:c.2743-485T=	XP_016860655.1:n.2743-485T=
XM_017005167.1:c.2197-485T=	XP_016860656.1:n.2197-485T=