Canonical Allele Identifier: CA1306213453

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944584A= , CM000664.2:g.168944584A=	GRCh38
NC_000002.11:g.169801094A= , CM000664.1:g.169801094A=	GRCh37
NC_000002.10:g.169509340A=	NCBI36
NG_007374.1:g.91740T=
NG_007374.2:g.91813T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.927+21T=	ENSP00000497165.1:n.927+21T=
ENST00000650372.1:c.2610+21T= MANE Select	ENSP00000497931.1:n.2610+21T=
ENST00000263817.6:c.2610+21T=	ENSP00000263817.6:n.2610+21T=
ENST00000439188.1:c.1299+21T=	ENSP00000416058.1:n.1299+21T=
NM_003742.2:c.2610+21T=	NP_003733.2:n.2610+21T=
XM_006712817.2:c.2652+21T=	XP_006712880.1:n.2652+21T=
XM_011512077.1:c.2712+21T=	XP_011510379.1:n.2712+21T=
XM_011512078.1:c.2712+21T=	XP_011510380.1:n.2712+21T=
XM_011512079.1:c.2712+21T=	XP_011510381.1:n.2712+21T=
XM_011512080.1:c.2712+21T=	XP_011510382.1:n.2712+21T=
XM_011512081.1:c.936+21T=	XP_011510383.1:n.936+21T=
NM_003742.4:c.2610+21T= MANE Select	NP_003733.2:n.2610+21T=
XM_006712817.3:c.2652+21T=	XP_006712880.1:n.2652+21T=
XM_011512077.2:c.2712+21T=	XP_011510379.1:n.2712+21T=
XM_011512078.2:c.2712+21T=	XP_011510380.1:n.2712+21T=
XM_011512080.2:c.2712+21T=	XP_011510382.1:n.2712+21T=
XM_011512081.2:c.936+21T=	XP_011510383.1:n.936+21T=
XM_017005165.1:c.2712+21T=	XP_016860654.1:n.2712+21T=
XM_017005166.1:c.1941+21T=	XP_016860655.1:n.1941+21T=
XM_017005167.1:c.1395+21T=	XP_016860656.1:n.1395+21T=