Canonical Allele Identifier: CA1306207173

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944692C= , CM000664.2:g.168944692C=	GRCh38
NC_000002.11:g.169801202C= , CM000664.1:g.169801202C=	GRCh37
NC_000002.10:g.169509448C=	NCBI36
NG_007374.1:g.91632G=
NG_007374.2:g.91705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.840G=	ENSP00000497165.1:p.Gly280=
ENST00000650372.1:c.2523G= MANE Select	ENSP00000497931.1:p.Gly841=
ENST00000263817.6:c.2523G=	ENSP00000263817.6:p.Gly841=
ENST00000439188.1:c.1212G=	ENSP00000416058.1:n.1212G=
NM_003742.2:c.2523G=	NP_003733.2:p.Gly841=
XM_006712817.2:c.2565G=	XP_006712880.1:p.Gly855=
XM_011512077.1:c.2625G=	XP_011510379.1:p.Gly875=
XM_011512078.1:c.2625G=	XP_011510380.1:p.Gly875=
XM_011512079.1:c.2625G=	XP_011510381.1:p.Gly875=
XM_011512080.1:c.2625G=	XP_011510382.1:p.Gly875=
XM_011512081.1:c.849G=	XP_011510383.1:p.Gly283=
NM_003742.4:c.2523G= MANE Select	NP_003733.2:p.Gly841=
XM_006712817.3:c.2565G=	XP_006712880.1:p.Gly855=
XM_011512077.2:c.2625G=	XP_011510379.1:p.Gly875=
XM_011512078.2:c.2625G=	XP_011510380.1:p.Gly875=
XM_011512080.2:c.2625G=	XP_011510382.1:p.Gly875=
XM_011512081.2:c.849G=	XP_011510383.1:p.Gly283=
XM_017005165.1:c.2625G=	XP_016860654.1:p.Gly875=
XM_017005166.1:c.1854G=	XP_016860655.1:p.Gly618=
XM_017005167.1:c.1308G=	XP_016860656.1:p.Gly436=