Canonical Allele Identifier: CA349126190
Gene: ABCB11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168944644C>G , CM000664.2:g.168944644C>G GRCh38
NC_000002.11:g.169801154C>G , CM000664.1:g.169801154C>G GRCh37
NC_000002.10:g.169509400C>G NCBI36
NG_007374.1:g.91680G>C
NG_007374.2:g.91753G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.888G>C ENSP00000497165.1:p.Leu296Phe
ENST00000650372.1:c.2571G>C MANE Select ENSP00000497931.1:p.Leu857Phe
ENST00000263817.6:c.2571G>C ENSP00000263817.6:p.Leu857Phe
ENST00000439188.1:c.1260G>C ENSP00000416058.1:n.1260G>C
NM_003742.2:c.2571G>C NP_003733.2:p.Leu857Phe
XM_006712817.2:c.2613G>C XP_006712880.1:p.Leu871Phe
XM_011512077.1:c.2673G>C XP_011510379.1:p.Leu891Phe
XM_011512078.1:c.2673G>C XP_011510380.1:p.Leu891Phe
XM_011512079.1:c.2673G>C XP_011510381.1:p.Leu891Phe
XM_011512080.1:c.2673G>C XP_011510382.1:p.Leu891Phe
XM_011512081.1:c.897G>C XP_011510383.1:p.Leu299Phe
NM_003742.4:c.2571G>C MANE Select NP_003733.2:p.Leu857Phe
XM_006712817.3:c.2613G>C XP_006712880.1:p.Leu871Phe
XM_011512077.2:c.2673G>C XP_011510379.1:p.Leu891Phe
XM_011512078.2:c.2673G>C XP_011510380.1:p.Leu891Phe
XM_011512080.2:c.2673G>C XP_011510382.1:p.Leu891Phe
XM_011512081.2:c.897G>C XP_011510383.1:p.Leu299Phe
XM_017005165.1:c.2673G>C XP_016860654.1:p.Leu891Phe
XM_017005166.1:c.1902G>C XP_016860655.1:p.Leu634Phe
XM_017005167.1:c.1356G>C XP_016860656.1:p.Leu452Phe