Canonical Allele Identifier: CA59870592
Gene: ABCB11 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16856247

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168927903C>T , CM000664.2:g.168927903C>T GRCh38
NC_000002.11:g.169784413C>T , CM000664.1:g.169784413C>T GRCh37
NC_000002.10:g.169492659C>T NCBI36
NG_007374.1:g.108421G>A
NG_007374.2:g.108494G>A

Transcript Alleles

HGVS Amino-acid change
NM_003742.2:c.3412-541G>A VV NP_003733.2:p.=
XM_006712817.2:c.3454-541G>A XP_006712880.1:p.=
XM_011512077.1:c.3514-541G>A XP_011510379.1:p.=
XM_011512078.1:c.3514-541G>A XP_011510380.1:p.=
XM_011512079.1:c.3514-541G>A XP_011510381.1:p.=
XM_011512081.1:c.1738-541G>A XP_011510383.1:p.=
NM_003742.4:c.3412-541G>A VV
XM_006712817.3:c.3454-541G>A
XM_011512077.2:c.3514-541G>A
XM_011512078.2:c.3514-541G>A
XM_011512081.2:c.1738-541G>A
XM_017005165.1:c.3514-541G>A XP_016860654.1:p.=
XM_017005166.1:c.2743-541G>A XP_016860655.1:p.=
XM_017005167.1:c.2197-541G>A XP_016860656.1:p.=
ENST00000263817.6:c.3412-541G>A ENSP00000263817.6:p.=
ENST00000439188.1:n.2101-613G>A ENSP00000416058.1:p.=