Canonical Allele Identifier: CA1723648218

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87566223A= , CM000669.2:g.87566223A=	GRCh38
NC_000007.13:g.87195539A= , CM000669.1:g.87195539A=	GRCh37
NC_000007.12:g.87033475A=	NCBI36
NG_011513.1:g.152026T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.549T=	ENSP00000265724.3:p.Asn183=
ENST00000622132.5:c.549T= MANE Select	ENSP00000478255.1:p.Asn183=
ENST00000265724.7:c.549T=	ENSP00000265724.3:p.Asn183=
ENST00000543898.5:c.357T=	ENSP00000444095.1:p.Asn119=
ENST00000622132.4:c.549T=	ENSP00000478255.1:p.Asn183=
NM_000927.4:c.549T=	NP_000918.2:p.Asn183=
NM_001348944.1:c.549T=	NP_001335873.1:p.Asn183=
NM_001348945.1:c.759T=	NP_001335874.1:p.Asn253=
NM_001348946.1:c.549T=	NP_001335875.1:p.Asn183=
NM_001348946.2:c.549T= MANE Select	NP_001335875.1:p.Asn183=
NM_000927.5:c.549T=	NP_000918.2:p.Asn183=
NM_001348944.2:c.549T=	NP_001335873.1:p.Asn183=
NM_001348945.2:c.759T=	NP_001335874.1:p.Asn253=