Canonical Allele Identifier: CA1306237658

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168990827A= , CM000664.2:g.168990827A=	GRCh38
NC_000002.11:g.169847337A= , CM000664.1:g.169847337A=	GRCh37
NC_000002.10:g.169555583A=	NCBI36
NG_007374.1:g.45497T=
NG_007374.2:g.45570T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650372.1:c.882T= MANE Select	ENSP00000497931.1:p.Phe294=
ENST00000263817.6:c.882T=	ENSP00000263817.6:p.Phe294=
NM_003742.2:c.882T=	NP_003733.2:p.Phe294=
XM_006712817.2:c.924T=	XP_006712880.1:p.Phe308=
XM_011512077.1:c.984T=	XP_011510379.1:p.Phe328=
XM_011512078.1:c.984T=	XP_011510380.1:p.Phe328=
XM_011512079.1:c.984T=	XP_011510381.1:p.Phe328=
XM_011512080.1:c.984T=	XP_011510382.1:p.Phe328=
NM_003742.4:c.882T= MANE Select	NP_003733.2:p.Phe294=
XM_006712817.3:c.924T=	XP_006712880.1:p.Phe308=
XM_011512077.2:c.984T=	XP_011510379.1:p.Phe328=
XM_011512078.2:c.984T=	XP_011510380.1:p.Phe328=
XM_011512080.2:c.984T=	XP_011510382.1:p.Phe328=
XM_017005165.1:c.984T=	XP_016860654.1:p.Phe328=
XM_017005166.1:c.213T=	XP_016860655.1:p.Phe71=