Canonical Allele Identifier: CA1723651392

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550129C= , CM000669.2:g.87550129C=	GRCh38
NC_000007.13:g.87179445C= , CM000669.1:g.87179445C=	GRCh37
NC_000007.12:g.87017381C=	NCBI36
NG_011513.1:g.168120G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1350+42G=	ENSP00000265724.3:n.1350+42G=
ENST00000622132.5:c.1350+42G= MANE Select	ENSP00000478255.1:n.1350+42G=
ENST00000265724.7:c.1350+42G=	ENSP00000265724.3:n.1350+42G=
ENST00000482527.1:n.30G=
ENST00000543898.5:c.1158+42G=	ENSP00000444095.1:n.1158+42G=
ENST00000622132.4:c.1350+42G=	ENSP00000478255.1:n.1350+42G=
NM_000927.4:c.1350+42G=	NP_000918.2:n.1350+42G=
NM_001348944.1:c.1350+42G=	NP_001335873.1:n.1350+42G=
NM_001348945.1:c.1560+42G=	NP_001335874.1:n.1560+42G=
NM_001348946.1:c.1350+42G=	NP_001335875.1:n.1350+42G=
NM_001348946.2:c.1350+42G= MANE Select	NP_001335875.1:n.1350+42G=
NM_000927.5:c.1350+42G=	NP_000918.2:n.1350+42G=
NM_001348944.2:c.1350+42G=	NP_001335873.1:n.1350+42G=
NM_001348945.2:c.1560+42G=	NP_001335874.1:n.1560+42G=