Canonical Allele Identifier: CA1306226499

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168973645G= , CM000664.2:g.168973645G=	GRCh38
NC_000002.11:g.169830155G= , CM000664.1:g.169830155G=	GRCh37
NC_000002.10:g.169538401G=	NCBI36
NG_007374.1:g.62679C=
NG_007374.2:g.62752C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650372.1:c.1434+70C= MANE Select	ENSP00000497931.1:n.1434+70C=
ENST00000263817.6:c.1434+70C=	ENSP00000263817.6:n.1434+70C=
NM_003742.2:c.1434+70C=	NP_003733.2:n.1434+70C=
XM_006712817.2:c.1476+70C=	XP_006712880.1:n.1476+70C=
XM_011512077.1:c.1536+70C=	XP_011510379.1:n.1536+70C=
XM_011512078.1:c.1536+70C=	XP_011510380.1:n.1536+70C=
XM_011512079.1:c.1536+70C=	XP_011510381.1:n.1536+70C=
XM_011512080.1:c.1536+70C=	XP_011510382.1:n.1536+70C=
NM_003742.4:c.1434+70C= MANE Select	NP_003733.2:n.1434+70C=
XM_006712817.3:c.1476+70C=	XP_006712880.1:n.1476+70C=
XM_011512077.2:c.1536+70C=	XP_011510379.1:n.1536+70C=
XM_011512078.2:c.1536+70C=	XP_011510380.1:n.1536+70C=
XM_011512080.2:c.1536+70C=	XP_011510382.1:n.1536+70C=
XM_017005165.1:c.1536+70C=	XP_016860654.1:n.1536+70C=
XM_017005166.1:c.765+70C=	XP_016860655.1:n.765+70C=
XM_017005167.1:c.219+70C=	XP_016860656.1:n.219+70C=