Canonical Allele Identifier: CA1723626729

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516520C= , CM000669.2:g.87516520C=	GRCh38
NC_000007.13:g.87145836C= , CM000669.1:g.87145836C=	GRCh37
NC_000007.12:g.86983772C=	NCBI36
NG_011513.1:g.201729G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3073G=	ENSP00000265724.3:p.Gly1025=
ENST00000622132.5:c.3073G= MANE Select	ENSP00000478255.1:p.Gly1025=
ENST00000265724.7:c.3073G=	ENSP00000265724.3:p.Gly1025=
ENST00000475929.5:n.229G=
ENST00000483831.1:n.631G=
ENST00000488737.6:n.715G=
ENST00000496821.5:n.701G=
ENST00000543898.5:c.2881G=	ENSP00000444095.1:p.Gly961=
ENST00000622132.4:c.3073G=	ENSP00000478255.1:p.Gly1025=
NM_000927.4:c.3073G=	NP_000918.2:p.Gly1025=
NM_001348944.1:c.3073G=	NP_001335873.1:p.Gly1025=
NM_001348945.1:c.3283G=	NP_001335874.1:p.Gly1095=
NM_001348946.1:c.3073G=	NP_001335875.1:p.Gly1025=
NM_001348946.2:c.3073G= MANE Select	NP_001335875.1:p.Gly1025=
NM_000927.5:c.3073G=	NP_000918.2:p.Gly1025=
NM_001348944.2:c.3073G=	NP_001335873.1:p.Gly1025=
NM_001348945.2:c.3283G=	NP_001335874.1:p.Gly1095=