Canonical Allele Identifier: CA2580581373

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600877A>T , CM000669.2:g.87600877A>T	GRCh38
NC_000007.13:g.87230193A>T , CM000669.1:g.87230193A>T	GRCh37
NC_000007.12:g.87068129A>T	NCBI36
NG_011513.1:g.117372T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-129T>A	ENSP00000265724.3:n.-129T>A
ENST00000622132.5:c.-129T>A MANE Select	ENSP00000478255.1:n.-129T>A
ENST00000265724.7:c.-129T>A	ENSP00000265724.3:n.-129T>A
ENST00000416177.1:c.-77-52T>A	ENSP00000399419.1:n.-77-52T>A
ENST00000476862.1:n.518T>A
ENST00000543898.5:c.-129T>A	ENSP00000444095.1:n.-129T>A
ENST00000622132.4:c.-129T>A	ENSP00000478255.1:n.-129T>A
NM_000927.4:c.-129T>A	NP_000918.2:n.-129T>A
NM_001348944.1:c.-77-52T>A	NP_001335873.1:n.-77-52T>A
NM_001348945.1:c.134-52T>A	NP_001335874.1:n.134-52T>A
NM_001348946.1:c.-129T>A	NP_001335875.1:n.-129T>A
NM_001348946.2:c.-129T>A MANE Select	NP_001335875.1:n.-129T>A
NM_000927.5:c.-129T>A	NP_000918.2:n.-129T>A
NM_001348944.2:c.-77-52T>A	NP_001335873.1:n.-77-52T>A
NM_001348945.2:c.134-52T>A	NP_001335874.1:n.134-52T>A