Canonical Allele Identifier: CA368043505

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87144572A>T (hg19) ; chr7:g.87515256A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515256A>T , CM000669.2:g.87515256A>T	GRCh38
NC_000007.13:g.87144572A>T , CM000669.1:g.87144572A>T	GRCh37
NC_000007.12:g.86982508A>T	NCBI36
NG_011513.1:g.202993T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3257T>A	ENSP00000265724.3:p.Phe1086Tyr
ENST00000622132.5:c.3257T>A MANE Select	ENSP00000478255.1:p.Phe1086Tyr
ENST00000265724.7:c.3257T>A	ENSP00000265724.3:p.Phe1086Tyr
ENST00000475929.5:n.413T>A
ENST00000488737.6:n.899T>A
ENST00000496821.5:n.885T>A
ENST00000543898.5:c.3065T>A	ENSP00000444095.1:p.Phe1022Tyr
ENST00000622132.4:c.3257T>A	ENSP00000478255.1:p.Phe1086Tyr
NM_000927.4:c.3257T>A	NP_000918.2:p.Phe1086Tyr
NM_001348944.1:c.3257T>A	NP_001335873.1:p.Phe1086Tyr
NM_001348945.1:c.3467T>A	NP_001335874.1:p.Phe1156Tyr
NM_001348946.1:c.3257T>A	NP_001335875.1:p.Phe1086Tyr
NM_001348946.2:c.3257T>A MANE Select	NP_001335875.1:p.Phe1086Tyr
NM_000927.5:c.3257T>A	NP_000918.2:p.Phe1086Tyr
NM_001348944.2:c.3257T>A	NP_001335873.1:p.Phe1086Tyr
NM_001348945.2:c.3467T>A	NP_001335874.1:p.Phe1156Tyr