Canonical Allele Identifier: CA2661804856

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168944523-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944523A>G , CM000664.2:g.168944523A>G	GRCh38
NC_000002.11:g.169801033A>G , CM000664.1:g.169801033A>G	GRCh37
NC_000002.10:g.169509279A>G	NCBI36
NG_007374.1:g.91801T>C
NG_007374.2:g.91874T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649448.1:c.927+82T>C	ENSP00000497165.1:n.927+82T>C
ENST00000650372.1:c.2610+82T>C MANE Select	ENSP00000497931.1:n.2610+82T>C
ENST00000263817.6:c.2610+82T>C	ENSP00000263817.6:n.2610+82T>C
ENST00000439188.1:c.1299+82T>C	ENSP00000416058.1:n.1299+82T>C
NM_003742.2:c.2610+82T>C	NP_003733.2:n.2610+82T>C
XM_006712817.2:c.2652+82T>C	XP_006712880.1:n.2652+82T>C
XM_011512077.1:c.2712+82T>C	XP_011510379.1:n.2712+82T>C
XM_011512078.1:c.2712+82T>C	XP_011510380.1:n.2712+82T>C
XM_011512079.1:c.2712+82T>C	XP_011510381.1:n.2712+82T>C
XM_011512080.1:c.2712+82T>C	XP_011510382.1:n.2712+82T>C
XM_011512081.1:c.936+82T>C	XP_011510383.1:n.936+82T>C
NM_003742.4:c.2610+82T>C MANE Select	NP_003733.2:n.2610+82T>C
XM_006712817.3:c.2652+82T>C	XP_006712880.1:n.2652+82T>C
XM_011512077.2:c.2712+82T>C	XP_011510379.1:n.2712+82T>C
XM_011512078.2:c.2712+82T>C	XP_011510380.1:n.2712+82T>C
XM_011512080.2:c.2712+82T>C	XP_011510382.1:n.2712+82T>C
XM_011512081.2:c.936+82T>C	XP_011510383.1:n.936+82T>C
XM_017005165.1:c.2712+82T>C	XP_016860654.1:n.2712+82T>C
XM_017005166.1:c.1941+82T>C	XP_016860655.1:n.1941+82T>C
XM_017005167.1:c.1395+82T>C	XP_016860656.1:n.1395+82T>C