Canonical Allele Identifier: CA1723621312

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503914C= , CM000669.2:g.87503914C=	GRCh38
NC_000007.13:g.87133230C= , CM000669.1:g.87133230C=	GRCh37
NC_000007.12:g.86971166C=	NCBI36
NG_011513.1:g.214335G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.*329G=	ENSP00000265724.3:n.*329G=
ENST00000622132.5:c.*329G= MANE Select	ENSP00000478255.1:n.*329G=
ENST00000265724.7:c.*329G=	ENSP00000265724.3:n.*329G=
ENST00000488737.6:n.1814G=
ENST00000543898.5:c.*329G=	ENSP00000444095.1:n.*329G=
ENST00000622132.4:c.*329G=	ENSP00000478255.1:n.*329G=
NM_000927.4:c.*329G=	NP_000918.2:n.*329G=
NM_001348944.1:c.*329G=	NP_001335873.1:n.*329G=
NM_001348945.1:c.*329G=	NP_001335874.1:n.*329G=
NM_001348946.1:c.*329G=	NP_001335875.1:n.*329G=
NM_001348946.2:c.*329G= MANE Select	NP_001335875.1:n.*329G=
NM_000927.5:c.*329G=	NP_000918.2:n.*329G=
NM_001348944.2:c.*329G=	NP_001335873.1:n.*329G=
NM_001348945.2:c.*329G=	NP_001335874.1:n.*329G=