Canonical Allele Identifier: CA1723626778

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516647G= , CM000669.2:g.87516647G=	GRCh38
NC_000007.13:g.87145963G= , CM000669.1:g.87145963G=	GRCh37
NC_000007.12:g.86983899G=	NCBI36
NG_011513.1:g.201602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2946C=	ENSP00000265724.3:p.Val982=
ENST00000622132.5:c.2946C= MANE Select	ENSP00000478255.1:p.Val982=
ENST00000265724.7:c.2946C=	ENSP00000265724.3:p.Val982=
ENST00000475929.5:n.102C=
ENST00000483831.1:n.504C=
ENST00000488737.6:n.588C=
ENST00000496821.5:n.574C=
ENST00000543898.5:c.2754C=	ENSP00000444095.1:p.Val918=
ENST00000622132.4:c.2946C=	ENSP00000478255.1:p.Val982=
NM_000927.4:c.2946C=	NP_000918.2:p.Val982=
NM_001348944.1:c.2946C=	NP_001335873.1:p.Val982=
NM_001348945.1:c.3156C=	NP_001335874.1:p.Val1052=
NM_001348946.1:c.2946C=	NP_001335875.1:p.Val982=
NM_001348946.2:c.2946C= MANE Select	NP_001335875.1:p.Val982=
NM_000927.5:c.2946C=	NP_000918.2:p.Val982=
NM_001348944.2:c.2946C=	NP_001335873.1:p.Val982=
NM_001348945.2:c.3156C=	NP_001335874.1:p.Val1052=