Canonical Allele Identifier: CA1723661790

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600877A= , CM000669.2:g.87600877A=	GRCh38
NC_000007.13:g.87230193A= , CM000669.1:g.87230193A=	GRCh37
NC_000007.12:g.87068129A=	NCBI36
NG_011513.1:g.117372T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-129T=	ENSP00000265724.3:n.-129T=
ENST00000622132.5:c.-129T= MANE Select	ENSP00000478255.1:n.-129T=
ENST00000265724.7:c.-129T=	ENSP00000265724.3:n.-129T=
ENST00000416177.1:c.-77-52T=	ENSP00000399419.1:n.-77-52T=
ENST00000476862.1:n.518T=
ENST00000543898.5:c.-129T=	ENSP00000444095.1:n.-129T=
ENST00000622132.4:c.-129T=	ENSP00000478255.1:n.-129T=
NM_000927.4:c.-129T=	NP_000918.2:n.-129T=
NM_001348944.1:c.-77-52T=	NP_001335873.1:n.-77-52T=
NM_001348945.1:c.134-52T=	NP_001335874.1:n.134-52T=
NM_001348946.1:c.-129T=	NP_001335875.1:n.-129T=
NM_001348946.2:c.-129T= MANE Select	NP_001335875.1:n.-129T=
NM_000927.5:c.-129T=	NP_000918.2:n.-129T=
NM_001348944.2:c.-77-52T=	NP_001335873.1:n.-77-52T=
NM_001348945.2:c.134-52T=	NP_001335874.1:n.134-52T=