Canonical Allele Identifier: CA1950954

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168924694T>C , CM000664.2:g.168924694T>C	GRCh38
NC_000002.11:g.169781204T>C , CM000664.1:g.169781204T>C	GRCh37
NC_000002.10:g.169489450T>C	NCBI36
NG_007374.1:g.111630A>G
NG_007374.2:g.111703A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.3728A>G MANE Select	NP_003733.2:p.Asp1243Gly
ENST00000650372.1:c.3728A>G MANE Select	ENSP00000497931.1:p.Asp1243Gly
NM_003742.2:c.3728A>G	NP_003733.2:p.Asp1243Gly
ENST00000263817.6:c.3728A>G	ENSP00000263817.6:p.Asp1243Gly
ENST00000439188.1:c.2345A>G	ENSP00000416058.1:n.2345A>G
ENST00000648875.1:c.189A>G
ENST00000649448.1:c.2105A>G	ENSP00000497165.1:p.Asp702Gly
XM_006712817.2:c.3770A>G	XP_006712880.1:p.Asp1257Gly
XM_006712817.3:c.3770A>G	XP_006712880.1:p.Asp1257Gly
XM_011512077.1:c.3830A>G	XP_011510379.1:p.Asp1277Gly
XM_011512077.2:c.3830A>G	XP_011510379.1:p.Asp1277Gly
XM_011512078.1:c.3830A>G	XP_011510380.1:p.Asp1277Gly
XM_011512078.2:c.3830A>G	XP_011510380.1:p.Asp1277Gly
XM_011512079.1:c.3830A>G	XP_011510381.1:p.Asp1277Gly
XM_011512081.1:c.2054A>G	XP_011510383.1:p.Asp685Gly
XM_011512081.2:c.2054A>G	XP_011510383.1:p.Asp685Gly
XM_017005165.1:c.3830A>G	XP_016860654.1:p.Asp1277Gly
XM_017005166.1:c.3059A>G	XP_016860655.1:p.Asp1020Gly
XM_017005167.1:c.2513A>G	XP_016860656.1:p.Asp838Gly