Canonical Allele Identifier: CA1306226584

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168973818A= , CM000664.2:g.168973818A=	GRCh38
NC_000002.11:g.169830328A= , CM000664.1:g.169830328A=	GRCh37
NC_000002.10:g.169538574A=	NCBI36
NG_007374.1:g.62506T=
NG_007374.2:g.62579T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.1331T= MANE Select	NP_003733.2:p.Val444=
ENST00000650372.1:c.1331T= MANE Select	ENSP00000497931.1:p.Val444=
NM_003742.2:c.1331T=	NP_003733.2:p.Val444=
ENST00000263817.6:c.1331T=	ENSP00000263817.6:p.Val444=
XM_006712817.2:c.1373T=	XP_006712880.1:p.Val458=
XM_006712817.3:c.1373T=	XP_006712880.1:p.Val458=
XM_011512077.1:c.1433T=	XP_011510379.1:p.Val478=
XM_011512077.2:c.1433T=	XP_011510379.1:p.Val478=
XM_011512078.1:c.1433T=	XP_011510380.1:p.Val478=
XM_011512078.2:c.1433T=	XP_011510380.1:p.Val478=
XM_011512079.1:c.1433T=	XP_011510381.1:p.Val478=
XM_011512080.1:c.1433T=	XP_011510382.1:p.Val478=
XM_011512080.2:c.1433T=	XP_011510382.1:p.Val478=
XM_017005165.1:c.1433T=	XP_016860654.1:p.Val478=
XM_017005166.1:c.662T=	XP_016860655.1:p.Val221=
XM_017005167.1:c.116T=	XP_016860656.1:p.Val39=