Canonical Allele Identifier: CA1306237789

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168990902A= , CM000664.2:g.168990902A=	GRCh38
NC_000002.11:g.169847412A= , CM000664.1:g.169847412A=	GRCh37
NC_000002.10:g.169555658A=	NCBI36
NG_007374.1:g.45422T=
NG_007374.2:g.45495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650372.1:c.807T= MANE Select	ENSP00000497931.1:p.Tyr269=
ENST00000263817.6:c.807T=	ENSP00000263817.6:p.Tyr269=
NM_003742.2:c.807T=	NP_003733.2:p.Tyr269=
XM_006712817.2:c.849T=	XP_006712880.1:p.Tyr283=
XM_011512077.1:c.909T=	XP_011510379.1:p.Tyr303=
XM_011512078.1:c.909T=	XP_011510380.1:p.Tyr303=
XM_011512079.1:c.909T=	XP_011510381.1:p.Tyr303=
XM_011512080.1:c.909T=	XP_011510382.1:p.Tyr303=
NM_003742.4:c.807T= MANE Select	NP_003733.2:p.Tyr269=
XM_006712817.3:c.849T=	XP_006712880.1:p.Tyr283=
XM_011512077.2:c.909T=	XP_011510379.1:p.Tyr303=
XM_011512078.2:c.909T=	XP_011510380.1:p.Tyr303=
XM_011512080.2:c.909T=	XP_011510382.1:p.Tyr303=
XM_017005165.1:c.909T=	XP_016860654.1:p.Tyr303=
XM_017005166.1:c.138T=	XP_016860655.1:p.Tyr46=