Canonical Allele Identifier: CA162099896

Gene: ABCB1

Linked Data

• dbSNP Id: rs1045642
• MyVariant Identifiers: chr7:g.87138645A>T (hg19) ; chr7:g.87509329A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87509329A>T , CM000669.2:g.87509329A>T	GRCh38
NC_000007.13:g.87138645A>T , CM000669.1:g.87138645A>T	GRCh37
NC_000007.12:g.86976581A>T	NCBI36
NG_011513.1:g.208920T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.3435T>A	ENSP00000265724.3:p.Ile1145=
ENST00000622132.5:c.3435T>A MANE Select	ENSP00000478255.1:p.Ile1145=
ENST00000265724.7:c.3435T>A	ENSP00000265724.3:p.Ile1145=
ENST00000475929.5:n.591T>A
ENST00000488737.6:n.1077T>A
ENST00000543898.5:c.3243T>A	ENSP00000444095.1:p.Ile1081=
ENST00000622132.4:c.3435T>A	ENSP00000478255.1:p.Ile1145=
NM_000927.4:c.3435T>A	NP_000918.2:p.Ile1145=
NM_001348944.1:c.3435T>A	NP_001335873.1:p.Ile1145=
NM_001348945.1:c.3645T>A	NP_001335874.1:p.Ile1215=
NM_001348946.1:c.3435T>A	NP_001335875.1:p.Ile1145=
NM_001348946.2:c.3435T>A MANE Select	NP_001335875.1:p.Ile1145=
NM_000927.5:c.3435T>A	NP_000918.2:p.Ile1145=
NM_001348944.2:c.3435T>A	NP_001335873.1:p.Ile1145=
NM_001348945.2:c.3645T>A	NP_001335874.1:p.Ile1215=