Canonical Allele Identifier: CA1306236644

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168996516A= , CM000664.2:g.168996516A=	GRCh38
NC_000002.11:g.169853026A= , CM000664.1:g.169853026A=	GRCh37
NC_000002.10:g.169561272A=	NCBI36
NG_007374.1:g.39808T=
NG_007374.2:g.39881T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650372.1:c.477+119T= MANE Select	ENSP00000497931.1:n.477+119T=
ENST00000263817.6:c.477+119T=	ENSP00000263817.6:n.477+119T=
NM_003742.2:c.477+119T=	NP_003733.2:n.477+119T=
XM_006712817.2:c.519+119T=	XP_006712880.1:n.519+119T=
XM_011512077.1:c.579+119T=	XP_011510379.1:n.579+119T=
XM_011512078.1:c.579+119T=	XP_011510380.1:n.579+119T=
XM_011512079.1:c.579+119T=	XP_011510381.1:n.579+119T=
XM_011512080.1:c.579+119T=	XP_011510382.1:n.579+119T=
NM_003742.4:c.477+119T= MANE Select	NP_003733.2:n.477+119T=
XM_006712817.3:c.519+119T=	XP_006712880.1:n.519+119T=
XM_011512077.2:c.579+119T=	XP_011510379.1:n.579+119T=
XM_011512078.2:c.579+119T=	XP_011510380.1:n.579+119T=
XM_011512080.2:c.579+119T=	XP_011510382.1:n.579+119T=
XM_017005165.1:c.579+119T=	XP_016860654.1:n.579+119T=