Canonical Allele Identifier: CA1306208152
Gene: ABCB11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168932451A= , CM000664.2:g.168932451A= GRCh38
NC_000002.11:g.169788961A= , CM000664.1:g.169788961A= GRCh37
NC_000002.10:g.169497207A= NCBI36
NG_007374.1:g.103873T=
NG_007374.2:g.103946T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.1456T= ENSP00000497165.1:p.Ser486=
ENST00000650372.1:c.3139T= MANE Select ENSP00000497931.1:p.Ser1047=
ENST00000263817.6:c.3139T= ENSP00000263817.6:p.Ser1047=
ENST00000439188.1:c.1828T= ENSP00000416058.1:n.1828T=
NM_003742.2:c.3139T= NP_003733.2:p.Ser1047=
XM_006712817.2:c.3181T= XP_006712880.1:p.Ser1061=
XM_011512077.1:c.3241T= XP_011510379.1:p.Ser1081=
XM_011512078.1:c.3241T= XP_011510380.1:p.Ser1081=
XM_011512079.1:c.3241T= XP_011510381.1:p.Ser1081=
XM_011512081.1:c.1465T= XP_011510383.1:p.Ser489=
NM_003742.4:c.3139T= MANE Select NP_003733.2:p.Ser1047=
XM_006712817.3:c.3181T= XP_006712880.1:p.Ser1061=
XM_011512077.2:c.3241T= XP_011510379.1:p.Ser1081=
XM_011512078.2:c.3241T= XP_011510380.1:p.Ser1081=
XM_011512081.2:c.1465T= XP_011510383.1:p.Ser489=
XM_017005165.1:c.3241T= XP_016860654.1:p.Ser1081=
XM_017005166.1:c.2470T= XP_016860655.1:p.Ser824=
XM_017005167.1:c.1924T= XP_016860656.1:p.Ser642=