Canonical Allele Identifier: CA1723628450

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520363G= , CM000669.2:g.87520363G=	GRCh38
NC_000007.13:g.87149679G= , CM000669.1:g.87149679G=	GRCh37
NC_000007.12:g.86987615G=	NCBI36
NG_011513.1:g.197886C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2786+413C=	ENSP00000265724.3:n.2786+413C=
ENST00000622132.5:c.2786+413C= MANE Select	ENSP00000478255.1:n.2786+413C=
ENST00000265724.7:c.2786+413C=	ENSP00000265724.3:n.2786+413C=
ENST00000483831.1:n.344+413C=
ENST00000488737.6:n.428+413C=
ENST00000496821.5:n.414+413C=
ENST00000543898.5:c.2594+413C=	ENSP00000444095.1:n.2594+413C=
ENST00000622132.4:c.2786+413C=	ENSP00000478255.1:n.2786+413C=
NM_000927.4:c.2786+413C=	NP_000918.2:n.2786+413C=
NM_001348944.1:c.2786+413C=	NP_001335873.1:n.2786+413C=
NM_001348945.1:c.2996+413C=	NP_001335874.1:n.2996+413C=
NM_001348946.1:c.2786+413C=	NP_001335875.1:n.2786+413C=
NM_001348946.2:c.2786+413C= MANE Select	NP_001335875.1:n.2786+413C=
NM_000927.5:c.2786+413C=	NP_000918.2:n.2786+413C=
NM_001348944.2:c.2786+413C=	NP_001335873.1:n.2786+413C=
NM_001348945.2:c.2996+413C=	NP_001335874.1:n.2996+413C=