Canonical Allele Identifier: CA1723626147

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515274A= , CM000669.2:g.87515274A=	GRCh38
NC_000007.13:g.87144590A= , CM000669.1:g.87144590A=	GRCh37
NC_000007.12:g.86982526A=	NCBI36
NG_011513.1:g.202975T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3239T=	ENSP00000265724.3:p.Val1080=
ENST00000622132.5:c.3239T= MANE Select	ENSP00000478255.1:p.Val1080=
ENST00000265724.7:c.3239T=	ENSP00000265724.3:p.Val1080=
ENST00000475929.5:n.395T=
ENST00000488737.6:n.881T=
ENST00000496821.5:n.867T=
ENST00000543898.5:c.3047T=	ENSP00000444095.1:p.Val1016=
ENST00000622132.4:c.3239T=	ENSP00000478255.1:p.Val1080=
NM_000927.4:c.3239T=	NP_000918.2:p.Val1080=
NM_001348944.1:c.3239T=	NP_001335873.1:p.Val1080=
NM_001348945.1:c.3449T=	NP_001335874.1:p.Val1150=
NM_001348946.1:c.3239T=	NP_001335875.1:p.Val1080=
NM_001348946.2:c.3239T= MANE Select	NP_001335875.1:p.Val1080=
NM_000927.5:c.3239T=	NP_000918.2:p.Val1080=
NM_001348944.2:c.3239T=	NP_001335873.1:p.Val1080=
NM_001348945.2:c.3449T=	NP_001335874.1:p.Val1150=