Canonical Allele Identifier: CA349126255
Gene: ABCB11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168944655G>T , CM000664.2:g.168944655G>T GRCh38
NC_000002.11:g.169801165G>T , CM000664.1:g.169801165G>T GRCh37
NC_000002.10:g.169509411G>T NCBI36
NG_007374.1:g.91669C>A
NG_007374.2:g.91742C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.877C>A ENSP00000497165.1:p.Pro293Thr
ENST00000650372.1:c.2560C>A MANE Select ENSP00000497931.1:p.Pro854Thr
ENST00000263817.6:c.2560C>A ENSP00000263817.6:p.Pro854Thr
ENST00000439188.1:c.1249C>A ENSP00000416058.1:n.1249C>A
NM_003742.2:c.2560C>A NP_003733.2:p.Pro854Thr
XM_006712817.2:c.2602C>A XP_006712880.1:p.Pro868Thr
XM_011512077.1:c.2662C>A XP_011510379.1:p.Pro888Thr
XM_011512078.1:c.2662C>A XP_011510380.1:p.Pro888Thr
XM_011512079.1:c.2662C>A XP_011510381.1:p.Pro888Thr
XM_011512080.1:c.2662C>A XP_011510382.1:p.Pro888Thr
XM_011512081.1:c.886C>A XP_011510383.1:p.Pro296Thr
NM_003742.4:c.2560C>A MANE Select NP_003733.2:p.Pro854Thr
XM_006712817.3:c.2602C>A XP_006712880.1:p.Pro868Thr
XM_011512077.2:c.2662C>A XP_011510379.1:p.Pro888Thr
XM_011512078.2:c.2662C>A XP_011510380.1:p.Pro888Thr
XM_011512080.2:c.2662C>A XP_011510382.1:p.Pro888Thr
XM_011512081.2:c.886C>A XP_011510383.1:p.Pro296Thr
XM_017005165.1:c.2662C>A XP_016860654.1:p.Pro888Thr
XM_017005166.1:c.1891C>A XP_016860655.1:p.Pro631Thr
XM_017005167.1:c.1345C>A XP_016860656.1:p.Pro449Thr