Canonical Allele Identifier: CA1723646667

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87544990T= , CM000669.2:g.87544990T=	GRCh38
NC_000007.13:g.87174306T= , CM000669.1:g.87174306T=	GRCh37
NC_000007.12:g.87012242T=	NCBI36
NG_011513.1:g.173259A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1897A=	ENSP00000265724.3:p.Asn633=
ENST00000622132.5:c.1897A= MANE Select	ENSP00000478255.1:p.Asn633=
ENST00000265724.7:c.1897A=	ENSP00000265724.3:p.Asn633=
ENST00000543898.5:c.1705A=	ENSP00000444095.1:p.Asn569=
ENST00000622132.4:c.1897A=	ENSP00000478255.1:p.Asn633=
NM_000927.4:c.1897A=	NP_000918.2:p.Asn633=
NM_001348944.1:c.1897A=	NP_001335873.1:p.Asn633=
NM_001348945.1:c.2107A=	NP_001335874.1:p.Asn703=
NM_001348946.1:c.1897A=	NP_001335875.1:p.Asn633=
NM_001348946.2:c.1897A= MANE Select	NP_001335875.1:p.Asn633=
NM_000927.5:c.1897A=	NP_000918.2:p.Asn633=
NM_001348944.2:c.1897A=	NP_001335873.1:p.Asn633=
NM_001348945.2:c.2107A=	NP_001335874.1:p.Asn703=