Canonical Allele Identifier: CA162124050

Gene: ABCB1

Linked Data

• dbSNP Id: rs554360805
• gnomAD v3: 7-87551411-A-T
• gnomAD v4: 7-87551411-A-T
• MyVariant Identifiers: chr7:g.87180727A>T (hg19) ; chr7:g.87551411A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87551411A>T , CM000669.2:g.87551411A>T	GRCh38
NC_000007.13:g.87180727A>T , CM000669.1:g.87180727A>T	GRCh37
NC_000007.12:g.87018663A>T	NCBI36
NG_011513.1:g.166838T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1000-573T>A	ENSP00000265724.3:n.1000-573T>A
ENST00000622132.5:c.1000-573T>A MANE Select	ENSP00000478255.1:n.1000-573T>A
ENST00000265724.7:c.1000-573T>A	ENSP00000265724.3:n.1000-573T>A
ENST00000543898.5:c.808-573T>A	ENSP00000444095.1:n.808-573T>A
ENST00000622132.4:c.1000-573T>A	ENSP00000478255.1:n.1000-573T>A
NM_000927.4:c.1000-573T>A	NP_000918.2:n.1000-573T>A
NM_001348944.1:c.1000-573T>A	NP_001335873.1:n.1000-573T>A
NM_001348945.1:c.1210-573T>A	NP_001335874.1:n.1210-573T>A
NM_001348946.1:c.1000-573T>A	NP_001335875.1:n.1000-573T>A
NM_001348946.2:c.1000-573T>A MANE Select	NP_001335875.1:n.1000-573T>A
NM_000927.5:c.1000-573T>A	NP_000918.2:n.1000-573T>A
NM_001348944.2:c.1000-573T>A	NP_001335873.1:n.1000-573T>A
NM_001348945.2:c.1210-573T>A	NP_001335874.1:n.1210-573T>A