Canonical Allele Identifier: CA10605968

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168970146C>T , CM000664.2:g.168970146C>T	GRCh38
NC_000002.11:g.169826656C>T , CM000664.1:g.169826656C>T	GRCh37
NC_000002.10:g.169534902C>T	NCBI36
NG_007374.1:g.66178G>A
NG_007374.2:g.66251G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.1708G>A MANE Select	NP_003733.2:p.Ala570Thr
ENST00000650372.1:c.1708G>A MANE Select	ENSP00000497931.1:p.Ala570Thr
NM_003742.2:c.1708G>A	NP_003733.2:p.Ala570Thr
ENST00000263817.6:c.1708G>A	ENSP00000263817.6:p.Ala570Thr
ENST00000439188.1:c.397G>A	ENSP00000416058.1:n.397G>A
ENST00000478354.1:n.446G>A
ENST00000649448.1:c.25G>A	ENSP00000497165.1:p.Ala9Thr
XM_006712817.2:c.1750G>A	XP_006712880.1:p.Ala584Thr
XM_006712817.3:c.1750G>A	XP_006712880.1:p.Ala584Thr
XM_011512077.1:c.1810G>A	XP_011510379.1:p.Ala604Thr
XM_011512077.2:c.1810G>A	XP_011510379.1:p.Ala604Thr
XM_011512078.1:c.1810G>A	XP_011510380.1:p.Ala604Thr
XM_011512078.2:c.1810G>A	XP_011510380.1:p.Ala604Thr
XM_011512079.1:c.1810G>A	XP_011510381.1:p.Ala604Thr
XM_011512080.1:c.1810G>A	XP_011510382.1:p.Ala604Thr
XM_011512080.2:c.1810G>A	XP_011510382.1:p.Ala604Thr
XM_011512081.1:c.34G>A	XP_011510383.1:p.Ala12Thr
XM_011512081.2:c.34G>A	XP_011510383.1:p.Ala12Thr
XM_017005165.1:c.1810G>A	XP_016860654.1:p.Ala604Thr
XM_017005166.1:c.1039G>A	XP_016860655.1:p.Ala347Thr
XM_017005167.1:c.493G>A	XP_016860656.1:p.Ala165Thr