Canonical Allele Identifier: CA429985466

Gene: ABCB11

Linked Data

• MyVariant Identifiers: chr2:g.169801441T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944931T>G , CM000664.2:g.168944931T>G	GRCh38
NC_000002.11:g.169801441T>G , CM000664.1:g.169801441T>G	GRCh37
NC_000002.10:g.169509687T>G	NCBI36
NG_007374.1:g.91393A>C
NG_007374.2:g.91466A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.691A>C	ENSP00000497165.1:p.Arg231=
ENST00000650372.1:c.2374A>C MANE Select	ENSP00000497931.1:p.Arg792=
ENST00000263817.6:c.2374A>C	ENSP00000263817.6:p.Arg792=
ENST00000439188.1:c.1063A>C	ENSP00000416058.1:n.1063A>C
NM_003742.2:c.2374A>C	NP_003733.2:p.Arg792=
XM_006712817.2:c.2416A>C	XP_006712880.1:p.Arg806=
XM_011512077.1:c.2476A>C	XP_011510379.1:p.Arg826=
XM_011512078.1:c.2476A>C	XP_011510380.1:p.Arg826=
XM_011512079.1:c.2476A>C	XP_011510381.1:p.Arg826=
XM_011512080.1:c.2476A>C	XP_011510382.1:p.Arg826=
XM_011512081.1:c.700A>C	XP_011510383.1:p.Arg234=
NM_003742.4:c.2374A>C MANE Select	NP_003733.2:p.Arg792=
XM_006712817.3:c.2416A>C	XP_006712880.1:p.Arg806=
XM_011512077.2:c.2476A>C	XP_011510379.1:p.Arg826=
XM_011512078.2:c.2476A>C	XP_011510380.1:p.Arg826=
XM_011512080.2:c.2476A>C	XP_011510382.1:p.Arg826=
XM_011512081.2:c.700A>C	XP_011510383.1:p.Arg234=
XM_017005165.1:c.2476A>C	XP_016860654.1:p.Arg826=
XM_017005166.1:c.1705A>C	XP_016860655.1:p.Arg569=
XM_017005167.1:c.1159A>C	XP_016860656.1:p.Arg387=