Canonical Allele Identifier: CA59898904
Gene: ABCB11 HGNC NCBI

Linked Data

dbSNP Id: rs72551308

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168996723dup , CM000664.2:g.168996723dup GRCh38
NC_000002.11:g.169853233dup , CM000664.1:g.169853233dup GRCh37
NC_000002.10:g.169561479dup NCBI36
NG_007374.1:g.39602dup
NG_007374.2:g.39675dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650372.1:c.390dup
ENST00000263817.6:c.390dup
NM_003742.2:c.390dup
XM_006712817.2:c.432dup
XM_011512077.1:c.492dup
XM_011512078.1:c.492dup
XM_011512079.1:c.492dup
XM_011512080.1:c.492dup
NM_003742.4:c.390dup
XM_006712817.3:c.432dup
XM_011512077.2:c.492dup
XM_011512078.2:c.492dup
XM_011512080.2:c.492dup
XM_017005165.1:c.492dup