Canonical Allele Identifier: CA1306201744
Gene: ABCB11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168927887A= , CM000664.2:g.168927887A= GRCh38
NC_000002.11:g.169784397A= , CM000664.1:g.169784397A= GRCh37
NC_000002.10:g.169492643A= NCBI36
NG_007374.1:g.108437T=
NG_007374.2:g.108510T=

Transcript Alleles

HGVS Amino-acid change
ENST00000649448.1:c.1789-525T= ENSP00000497165.1:n.1789-525T=
ENST00000650372.1:c.3412-525T= MANE Select ENSP00000497931.1:n.3412-525T=
ENST00000263817.6:c.3412-525T= ENSP00000263817.6:n.3412-525T=
ENST00000439188.1:c.2101-597T= ENSP00000416058.1:n.2101-597T=
NM_003742.2:c.3412-525T= NP_003733.2:n.3412-525T=
XM_006712817.2:c.3454-525T= XP_006712880.1:n.3454-525T=
XM_011512077.1:c.3514-525T= XP_011510379.1:n.3514-525T=
XM_011512078.1:c.3514-525T= XP_011510380.1:n.3514-525T=
XM_011512079.1:c.3514-525T= XP_011510381.1:n.3514-525T=
XM_011512081.1:c.1738-525T= XP_011510383.1:n.1738-525T=
NM_003742.4:c.3412-525T= MANE Select NP_003733.2:n.3412-525T=
XM_006712817.3:c.3454-525T= XP_006712880.1:n.3454-525T=
XM_011512077.2:c.3514-525T= XP_011510379.1:n.3514-525T=
XM_011512078.2:c.3514-525T= XP_011510380.1:n.3514-525T=
XM_011512081.2:c.1738-525T= XP_011510383.1:n.1738-525T=
XM_017005165.1:c.3514-525T= XP_016860654.1:n.3514-525T=
XM_017005166.1:c.2743-525T= XP_016860655.1:n.2743-525T=
XM_017005167.1:c.2197-525T= XP_016860656.1:n.2197-525T=