Canonical Allele Identifier: CA1306237636

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168990819T= , CM000664.2:g.168990819T=	GRCh38
NC_000002.11:g.169847329T= , CM000664.1:g.169847329T=	GRCh37
NC_000002.10:g.169555575T=	NCBI36
NG_007374.1:g.45505A=
NG_007374.2:g.45578A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.890A= MANE Select	NP_003733.2:p.Glu297=
ENST00000650372.1:c.890A= MANE Select	ENSP00000497931.1:p.Glu297=
NM_003742.2:c.890A=	NP_003733.2:p.Glu297=
ENST00000263817.6:c.890A=	ENSP00000263817.6:p.Glu297=
XM_006712817.2:c.932A=	XP_006712880.1:p.Glu311=
XM_006712817.3:c.932A=	XP_006712880.1:p.Glu311=
XM_011512077.1:c.992A=	XP_011510379.1:p.Glu331=
XM_011512077.2:c.992A=	XP_011510379.1:p.Glu331=
XM_011512078.1:c.992A=	XP_011510380.1:p.Glu331=
XM_011512078.2:c.992A=	XP_011510380.1:p.Glu331=
XM_011512079.1:c.992A=	XP_011510381.1:p.Glu331=
XM_011512080.1:c.992A=	XP_011510382.1:p.Glu331=
XM_011512080.2:c.992A=	XP_011510382.1:p.Glu331=
XM_017005165.1:c.992A=	XP_016860654.1:p.Glu331=
XM_017005166.1:c.221A=	XP_016860655.1:p.Glu74=