Canonical Allele Identifier: CA1306201669
Gene: ABCB11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168927771C= , CM000664.2:g.168927771C= GRCh38
NC_000002.11:g.169784281C= , CM000664.1:g.169784281C= GRCh37
NC_000002.10:g.169492527C= NCBI36
NG_007374.1:g.108553G=
NG_007374.2:g.108626G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.1789-409G= ENSP00000497165.1:n.1789-409G=
ENST00000650372.1:c.3412-409G= MANE Select ENSP00000497931.1:n.3412-409G=
ENST00000263817.6:c.3412-409G= ENSP00000263817.6:n.3412-409G=
ENST00000439188.1:c.2101-481G= ENSP00000416058.1:n.2101-481G=
NM_003742.2:c.3412-409G= NP_003733.2:n.3412-409G=
XM_006712817.2:c.3454-409G= XP_006712880.1:n.3454-409G=
XM_011512077.1:c.3514-409G= XP_011510379.1:n.3514-409G=
XM_011512078.1:c.3514-409G= XP_011510380.1:n.3514-409G=
XM_011512079.1:c.3514-409G= XP_011510381.1:n.3514-409G=
XM_011512081.1:c.1738-409G= XP_011510383.1:n.1738-409G=
NM_003742.4:c.3412-409G= MANE Select NP_003733.2:n.3412-409G=
XM_006712817.3:c.3454-409G= XP_006712880.1:n.3454-409G=
XM_011512077.2:c.3514-409G= XP_011510379.1:n.3514-409G=
XM_011512078.2:c.3514-409G= XP_011510380.1:n.3514-409G=
XM_011512081.2:c.1738-409G= XP_011510383.1:n.1738-409G=
XM_017005165.1:c.3514-409G= XP_016860654.1:n.3514-409G=
XM_017005166.1:c.2743-409G= XP_016860655.1:n.2743-409G=
XM_017005167.1:c.2197-409G= XP_016860656.1:n.2197-409G=