Canonical Allele Identifier: CA1723626863

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516803C= , CM000669.2:g.87516803C=	GRCh38
NC_000007.13:g.87146119C= , CM000669.1:g.87146119C=	GRCh37
NC_000007.12:g.86984055C=	NCBI36
NG_011513.1:g.201446G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2928-138G=	ENSP00000265724.3:n.2928-138G=
ENST00000622132.5:c.2928-138G= MANE Select	ENSP00000478255.1:n.2928-138G=
ENST00000265724.7:c.2928-138G=	ENSP00000265724.3:n.2928-138G=
ENST00000475929.5:n.84-138G=
ENST00000483831.1:n.486-138G=
ENST00000488737.6:n.570-138G=
ENST00000496821.5:n.556-138G=
ENST00000543898.5:c.2736-138G=	ENSP00000444095.1:n.2736-138G=
ENST00000622132.4:c.2928-138G=	ENSP00000478255.1:n.2928-138G=
NM_000927.4:c.2928-138G=	NP_000918.2:n.2928-138G=
NM_001348944.1:c.2928-138G=	NP_001335873.1:n.2928-138G=
NM_001348945.1:c.3138-138G=	NP_001335874.1:n.3138-138G=
NM_001348946.1:c.2928-138G=	NP_001335875.1:n.2928-138G=
NM_001348946.2:c.2928-138G= MANE Select	NP_001335875.1:n.2928-138G=
NM_000927.5:c.2928-138G=	NP_000918.2:n.2928-138G=
NM_001348944.2:c.2928-138G=	NP_001335873.1:n.2928-138G=
NM_001348945.2:c.3138-138G=	NP_001335874.1:n.3138-138G=