Canonical Allele Identifier: CA429985178

Gene: ABCB11

Linked Data

• MyVariant Identifiers: chr2:g.169801124T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944614T>C , CM000664.2:g.168944614T>C	GRCh38
NC_000002.11:g.169801124T>C , CM000664.1:g.169801124T>C	GRCh37
NC_000002.10:g.169509370T>C	NCBI36
NG_007374.1:g.91710A>G
NG_007374.2:g.91783A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.918A>G	ENSP00000497165.1:p.Gln306=
ENST00000650372.1:c.2601A>G MANE Select	ENSP00000497931.1:p.Gln867=
ENST00000263817.6:c.2601A>G	ENSP00000263817.6:p.Gln867=
ENST00000439188.1:c.1290A>G	ENSP00000416058.1:n.1290A>G
NM_003742.2:c.2601A>G	NP_003733.2:p.Gln867=
XM_006712817.2:c.2643A>G	XP_006712880.1:p.Gln881=
XM_011512077.1:c.2703A>G	XP_011510379.1:p.Gln901=
XM_011512078.1:c.2703A>G	XP_011510380.1:p.Gln901=
XM_011512079.1:c.2703A>G	XP_011510381.1:p.Gln901=
XM_011512080.1:c.2703A>G	XP_011510382.1:p.Gln901=
XM_011512081.1:c.927A>G	XP_011510383.1:p.Gln309=
NM_003742.4:c.2601A>G MANE Select	NP_003733.2:p.Gln867=
XM_006712817.3:c.2643A>G	XP_006712880.1:p.Gln881=
XM_011512077.2:c.2703A>G	XP_011510379.1:p.Gln901=
XM_011512078.2:c.2703A>G	XP_011510380.1:p.Gln901=
XM_011512080.2:c.2703A>G	XP_011510382.1:p.Gln901=
XM_011512081.2:c.927A>G	XP_011510383.1:p.Gln309=
XM_017005165.1:c.2703A>G	XP_016860654.1:p.Gln901=
XM_017005166.1:c.1932A>G	XP_016860655.1:p.Gln644=
XM_017005167.1:c.1386A>G	XP_016860656.1:p.Gln462=