Canonical Allele Identifier: CA1306236774

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168996655G= , CM000664.2:g.168996655G=	GRCh38
NC_000002.11:g.169853165G= , CM000664.1:g.169853165G=	GRCh37
NC_000002.10:g.169561411G=	NCBI36
NG_007374.1:g.39669C=
NG_007374.2:g.39742C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650372.1:c.457C= MANE Select	ENSP00000497931.1:p.Leu153=
ENST00000263817.6:c.457C=	ENSP00000263817.6:p.Leu153=
NM_003742.2:c.457C=	NP_003733.2:p.Leu153=
XM_006712817.2:c.499C=	XP_006712880.1:p.Leu167=
XM_011512077.1:c.559C=	XP_011510379.1:p.Leu187=
XM_011512078.1:c.559C=	XP_011510380.1:p.Leu187=
XM_011512079.1:c.559C=	XP_011510381.1:p.Leu187=
XM_011512080.1:c.559C=	XP_011510382.1:p.Leu187=
NM_003742.4:c.457C= MANE Select	NP_003733.2:p.Leu153=
XM_006712817.3:c.499C=	XP_006712880.1:p.Leu167=
XM_011512077.2:c.559C=	XP_011510379.1:p.Leu187=
XM_011512078.2:c.559C=	XP_011510380.1:p.Leu187=
XM_011512080.2:c.559C=	XP_011510382.1:p.Leu187=
XM_017005165.1:c.559C=	XP_016860654.1:p.Leu187=