Canonical Allele Identifier: CA349122462
Gene: ABCB11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168932453A>T , CM000664.2:g.168932453A>T GRCh38
NC_000002.11:g.169788963A>T , CM000664.1:g.169788963A>T GRCh37
NC_000002.10:g.169497209A>T NCBI36
NG_007374.1:g.103871T>A
NG_007374.2:g.103944T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.1454T>A ENSP00000497165.1:p.Ile485Lys
ENST00000650372.1:c.3137T>A MANE Select ENSP00000497931.1:p.Ile1046Lys
ENST00000263817.6:c.3137T>A ENSP00000263817.6:p.Ile1046Lys
ENST00000439188.1:c.1826T>A ENSP00000416058.1:n.1826T>A
NM_003742.2:c.3137T>A NP_003733.2:p.Ile1046Lys
XM_006712817.2:c.3179T>A XP_006712880.1:p.Ile1060Lys
XM_011512077.1:c.3239T>A XP_011510379.1:p.Ile1080Lys
XM_011512078.1:c.3239T>A XP_011510380.1:p.Ile1080Lys
XM_011512079.1:c.3239T>A XP_011510381.1:p.Ile1080Lys
XM_011512081.1:c.1463T>A XP_011510383.1:p.Ile488Lys
NM_003742.4:c.3137T>A MANE Select NP_003733.2:p.Ile1046Lys
XM_006712817.3:c.3179T>A XP_006712880.1:p.Ile1060Lys
XM_011512077.2:c.3239T>A XP_011510379.1:p.Ile1080Lys
XM_011512078.2:c.3239T>A XP_011510380.1:p.Ile1080Lys
XM_011512081.2:c.1463T>A XP_011510383.1:p.Ile488Lys
XM_017005165.1:c.3239T>A XP_016860654.1:p.Ile1080Lys
XM_017005166.1:c.2468T>A XP_016860655.1:p.Ile823Lys
XM_017005167.1:c.1922T>A XP_016860656.1:p.Ile641Lys