Canonical Allele Identifier: CA1723628642

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520777T= , CM000669.2:g.87520777T=	GRCh38
NC_000007.13:g.87150093T= , CM000669.1:g.87150093T=	GRCh37
NC_000007.12:g.86988029T=	NCBI36
NG_011513.1:g.197472A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2785A=	ENSP00000265724.3:p.Arg929=
ENST00000622132.5:c.2785A= MANE Select	ENSP00000478255.1:p.Arg929=
ENST00000265724.7:c.2785A=	ENSP00000265724.3:p.Arg929=
ENST00000483831.1:n.343A=
ENST00000488737.6:n.427A=
ENST00000496821.5:n.413A=
ENST00000543898.5:c.2593A=	ENSP00000444095.1:p.Arg865=
ENST00000622132.4:c.2785A=	ENSP00000478255.1:p.Arg929=
NM_000927.4:c.2785A=	NP_000918.2:p.Arg929=
NM_001348944.1:c.2785A=	NP_001335873.1:p.Arg929=
NM_001348945.1:c.2995A=	NP_001335874.1:p.Arg999=
NM_001348946.1:c.2785A=	NP_001335875.1:p.Arg929=
NM_001348946.2:c.2785A= MANE Select	NP_001335875.1:p.Arg929=
NM_000927.5:c.2785A=	NP_000918.2:p.Arg929=
NM_001348944.2:c.2785A=	NP_001335873.1:p.Arg929=
NM_001348945.2:c.2995A=	NP_001335874.1:p.Arg999=