Canonical Allele Identifier: CA1951635

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168976604G>A , CM000664.2:g.168976604G>A	GRCh38
NC_000002.11:g.169833114G>A , CM000664.1:g.169833114G>A	GRCh37
NC_000002.10:g.169541360G>A	NCBI36
NG_007374.1:g.59720C>T
NG_007374.2:g.59793C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.1281C>T MANE Select	NP_003733.2:p.Phe427=
ENST00000650372.1:c.1281C>T MANE Select	ENSP00000497931.1:p.Phe427=
NM_003742.2:c.1281C>T	NP_003733.2:p.Phe427=
ENST00000263817.6:c.1281C>T	ENSP00000263817.6:p.Phe427=
XM_006712817.2:c.1323C>T	XP_006712880.1:p.Phe441=
XM_006712817.3:c.1323C>T	XP_006712880.1:p.Phe441=
XM_011512077.1:c.1383C>T	XP_011510379.1:p.Phe461=
XM_011512077.2:c.1383C>T	XP_011510379.1:p.Phe461=
XM_011512078.1:c.1383C>T	XP_011510380.1:p.Phe461=
XM_011512078.2:c.1383C>T	XP_011510380.1:p.Phe461=
XM_011512079.1:c.1383C>T	XP_011510381.1:p.Phe461=
XM_011512080.1:c.1383C>T	XP_011510382.1:p.Phe461=
XM_011512080.2:c.1383C>T	XP_011510382.1:p.Phe461=
XM_017005165.1:c.1383C>T	XP_016860654.1:p.Phe461=
XM_017005166.1:c.612C>T	XP_016860655.1:p.Phe204=
XM_017005167.1:c.66C>T	XP_016860656.1:p.Phe22=