Canonical Allele Identifier: CA456349298

Gene: ABCB1

Linked Data

• dbSNP Id: rs1815178471
• MyVariant Identifiers: chr7:g.87144565G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515249G>A , CM000669.2:g.87515249G>A	GRCh38
NC_000007.13:g.87144565G>A , CM000669.1:g.87144565G>A	GRCh37
NC_000007.12:g.86982501G>A	NCBI36
NG_011513.1:g.203000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3264C>T	ENSP00000265724.3:p.Asp1088=
ENST00000622132.5:c.3264C>T MANE Select	ENSP00000478255.1:p.Asp1088=
ENST00000265724.7:c.3264C>T	ENSP00000265724.3:p.Asp1088=
ENST00000475929.5:n.420C>T
ENST00000488737.6:n.906C>T
ENST00000496821.5:n.892C>T
ENST00000543898.5:c.3072C>T	ENSP00000444095.1:p.Asp1024=
ENST00000622132.4:c.3264C>T	ENSP00000478255.1:p.Asp1088=
NM_000927.4:c.3264C>T	NP_000918.2:p.Asp1088=
NM_001348944.1:c.3264C>T	NP_001335873.1:p.Asp1088=
NM_001348945.1:c.3474C>T	NP_001335874.1:p.Asp1158=
NM_001348946.1:c.3264C>T	NP_001335875.1:p.Asp1088=
NM_001348946.2:c.3264C>T MANE Select	NP_001335875.1:p.Asp1088=
NM_000927.5:c.3264C>T	NP_000918.2:p.Asp1088=
NM_001348944.2:c.3264C>T	NP_001335873.1:p.Asp1088=
NM_001348945.2:c.3474C>T	NP_001335874.1:p.Asp1158=