Canonical Allele Identifier: CA1306207506
Gene: ABCB11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168944993T= , CM000664.2:g.168944993T= GRCh38
NC_000002.11:g.169801503T= , CM000664.1:g.169801503T= GRCh37
NC_000002.10:g.169509749T= NCBI36
NG_007374.1:g.91331A=
NG_007374.2:g.91404A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.661-32A= ENSP00000497165.1:n.661-32A=
ENST00000650372.1:c.2344-32A= MANE Select ENSP00000497931.1:n.2344-32A=
ENST00000263817.6:c.2344-32A= ENSP00000263817.6:n.2344-32A=
ENST00000439188.1:c.1033-32A= ENSP00000416058.1:n.1033-32A=
NM_003742.2:c.2344-32A= NP_003733.2:n.2344-32A=
XM_006712817.2:c.2386-32A= XP_006712880.1:n.2386-32A=
XM_011512077.1:c.2446-32A= XP_011510379.1:n.2446-32A=
XM_011512078.1:c.2446-32A= XP_011510380.1:n.2446-32A=
XM_011512079.1:c.2446-32A= XP_011510381.1:n.2446-32A=
XM_011512080.1:c.2446-32A= XP_011510382.1:n.2446-32A=
XM_011512081.1:c.670-32A= XP_011510383.1:n.670-32A=
NM_003742.4:c.2344-32A= MANE Select NP_003733.2:n.2344-32A=
XM_006712817.3:c.2386-32A= XP_006712880.1:n.2386-32A=
XM_011512077.2:c.2446-32A= XP_011510379.1:n.2446-32A=
XM_011512078.2:c.2446-32A= XP_011510380.1:n.2446-32A=
XM_011512080.2:c.2446-32A= XP_011510382.1:n.2446-32A=
XM_011512081.2:c.670-32A= XP_011510383.1:n.670-32A=
XM_017005165.1:c.2446-32A= XP_016860654.1:n.2446-32A=
XM_017005166.1:c.1675-32A= XP_016860655.1:n.1675-32A=
XM_017005167.1:c.1129-32A= XP_016860656.1:n.1129-32A=