Canonical Allele Identifier: CA1950957

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168924730C>T , CM000664.2:g.168924730C>T	GRCh38
NC_000002.11:g.169781240C>T , CM000664.1:g.169781240C>T	GRCh37
NC_000002.10:g.169489486C>T	NCBI36
NG_007374.1:g.111594G>A
NG_007374.2:g.111667G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.3692G>A MANE Select	NP_003733.2:p.Arg1231Gln
ENST00000650372.1:c.3692G>A MANE Select	ENSP00000497931.1:p.Arg1231Gln
NM_003742.2:c.3692G>A	NP_003733.2:p.Arg1231Gln
ENST00000263817.6:c.3692G>A	ENSP00000263817.6:p.Arg1231Gln
ENST00000439188.1:c.2309G>A	ENSP00000416058.1:n.2309G>A
ENST00000648875.1:c.153G>A
ENST00000649448.1:c.2069G>A	ENSP00000497165.1:p.Arg690Gln
XM_006712817.2:c.3734G>A	XP_006712880.1:p.Arg1245Gln
XM_006712817.3:c.3734G>A	XP_006712880.1:p.Arg1245Gln
XM_011512077.1:c.3794G>A	XP_011510379.1:p.Arg1265Gln
XM_011512077.2:c.3794G>A	XP_011510379.1:p.Arg1265Gln
XM_011512078.1:c.3794G>A	XP_011510380.1:p.Arg1265Gln
XM_011512078.2:c.3794G>A	XP_011510380.1:p.Arg1265Gln
XM_011512079.1:c.3794G>A	XP_011510381.1:p.Arg1265Gln
XM_011512081.1:c.2018G>A	XP_011510383.1:p.Arg673Gln
XM_011512081.2:c.2018G>A	XP_011510383.1:p.Arg673Gln
XM_017005165.1:c.3794G>A	XP_016860654.1:p.Arg1265Gln
XM_017005166.1:c.3023G>A	XP_016860655.1:p.Arg1008Gln
XM_017005167.1:c.2477G>A	XP_016860656.1:p.Arg826Gln