Canonical Allele Identifier: CA456449998

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87179362A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550046A>T , CM000669.2:g.87550046A>T	GRCh38
NC_000007.13:g.87179362A>T , CM000669.1:g.87179362A>T	GRCh37
NC_000007.12:g.87017298A>T	NCBI36
NG_011513.1:g.168203T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1359T>A	ENSP00000265724.3:p.Val453=
ENST00000622132.5:c.1359T>A MANE Select	ENSP00000478255.1:p.Val453=
ENST00000265724.7:c.1359T>A	ENSP00000265724.3:p.Val453=
ENST00000482527.1:n.113T>A
ENST00000543898.5:c.1167T>A	ENSP00000444095.1:p.Val389=
ENST00000622132.4:c.1359T>A	ENSP00000478255.1:p.Val453=
NM_000927.4:c.1359T>A	NP_000918.2:p.Val453=
NM_001348944.1:c.1359T>A	NP_001335873.1:p.Val453=
NM_001348945.1:c.1569T>A	NP_001335874.1:p.Val523=
NM_001348946.1:c.1359T>A	NP_001335875.1:p.Val453=
NM_001348946.2:c.1359T>A MANE Select	NP_001335875.1:p.Val453=
NM_000927.5:c.1359T>A	NP_000918.2:p.Val453=
NM_001348944.2:c.1359T>A	NP_001335873.1:p.Val453=
NM_001348945.2:c.1569T>A	NP_001335874.1:p.Val523=