Canonical Allele Identifier: CA1723626359

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515720A= , CM000669.2:g.87515720A=	GRCh38
NC_000007.13:g.87145036A= , CM000669.1:g.87145036A=	GRCh37
NC_000007.12:g.86982972A=	NCBI36
NG_011513.1:g.202529T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3085-292T=	ENSP00000265724.3:n.3085-292T=
ENST00000622132.5:c.3085-292T= MANE Select	ENSP00000478255.1:n.3085-292T=
ENST00000265724.7:c.3085-292T=	ENSP00000265724.3:n.3085-292T=
ENST00000475929.5:n.241-292T=
ENST00000488737.6:n.727-292T=
ENST00000496821.5:n.713-292T=
ENST00000543898.5:c.2893-292T=	ENSP00000444095.1:n.2893-292T=
ENST00000622132.4:c.3085-292T=	ENSP00000478255.1:n.3085-292T=
NM_000927.4:c.3085-292T=	NP_000918.2:n.3085-292T=
NM_001348944.1:c.3085-292T=	NP_001335873.1:n.3085-292T=
NM_001348945.1:c.3295-292T=	NP_001335874.1:n.3295-292T=
NM_001348946.1:c.3085-292T=	NP_001335875.1:n.3085-292T=
NM_001348946.2:c.3085-292T= MANE Select	NP_001335875.1:n.3085-292T=
NM_000927.5:c.3085-292T=	NP_000918.2:n.3085-292T=
NM_001348944.2:c.3085-292T=	NP_001335873.1:n.3085-292T=
NM_001348945.2:c.3295-292T=	NP_001335874.1:n.3295-292T=