Canonical Allele Identifier: CA1723628649

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520793A= , CM000669.2:g.87520793A=	GRCh38
NC_000007.13:g.87150109A= , CM000669.1:g.87150109A=	GRCh37
NC_000007.12:g.86988045A=	NCBI36
NG_011513.1:g.197456T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2769T=	ENSP00000265724.3:p.Ser923=
ENST00000622132.5:c.2769T= MANE Select	ENSP00000478255.1:p.Ser923=
ENST00000265724.7:c.2769T=	ENSP00000265724.3:p.Ser923=
ENST00000483831.1:n.327T=
ENST00000488737.6:n.411T=
ENST00000496821.5:n.397T=
ENST00000543898.5:c.2577T=	ENSP00000444095.1:p.Ser859=
ENST00000622132.4:c.2769T=	ENSP00000478255.1:p.Ser923=
NM_000927.4:c.2769T=	NP_000918.2:p.Ser923=
NM_001348944.1:c.2769T=	NP_001335873.1:p.Ser923=
NM_001348945.1:c.2979T=	NP_001335874.1:p.Ser993=
NM_001348946.1:c.2769T=	NP_001335875.1:p.Ser923=
NM_001348946.2:c.2769T= MANE Select	NP_001335875.1:p.Ser923=
NM_000927.5:c.2769T=	NP_000918.2:p.Ser923=
NM_001348944.2:c.2769T=	NP_001335873.1:p.Ser923=
NM_001348945.2:c.2979T=	NP_001335874.1:p.Ser993=