Canonical Allele Identifier: CA2661802609

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168923176-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168923176A>C , CM000664.2:g.168923176A>C	GRCh38
NC_000002.11:g.169779686A>C , CM000664.1:g.169779686A>C	GRCh37
NC_000002.10:g.169487932A>C	NCBI36
NG_007374.1:g.113148T>G
NG_007374.2:g.113221T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000648875.1:c.226+1481T>G
ENST00000649448.1:c.2789T>G	ENSP00000497165.1:n.2789T>G
ENST00000650372.1:c.*446T>G MANE Select	ENSP00000497931.1:n.*446T>G
ENST00000263817.6:c.*446T>G	ENSP00000263817.6:n.*446T>G
NM_003742.2:c.*446T>G	NP_003733.2:n.*446T>G
XM_006712817.2:c.*446T>G	XP_006712880.1:n.*446T>G
XM_011512077.1:c.*446T>G	XP_011510379.1:n.*446T>G
XM_011512078.1:c.*400T>G	XP_011510380.1:n.*400T>G
XM_011512079.1:c.*446T>G	XP_011510381.1:n.*446T>G
XM_011512081.1:c.*446T>G	XP_011510383.1:n.*446T>G
NM_003742.4:c.*446T>G MANE Select	NP_003733.2:n.*446T>G
XM_006712817.3:c.*446T>G	XP_006712880.1:n.*446T>G
XM_011512077.2:c.*446T>G	XP_011510379.1:n.*446T>G
XM_011512078.2:c.*400T>G	XP_011510380.1:n.*400T>G
XM_011512081.2:c.*446T>G	XP_011510383.1:n.*446T>G
XM_017005165.1:c.3867+1481T>G	XP_016860654.1:n.3867+1481T>G
XM_017005166.1:c.*446T>G	XP_016860655.1:n.*446T>G
XM_017005167.1:c.*446T>G	XP_016860656.1:n.*446T>G