Canonical Allele Identifier: CA456351239

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87150093T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520777T>G , CM000669.2:g.87520777T>G	GRCh38
NC_000007.13:g.87150093T>G , CM000669.1:g.87150093T>G	GRCh37
NC_000007.12:g.86988029T>G	NCBI36
NG_011513.1:g.197472A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2785A>C	ENSP00000265724.3:p.Arg929=
ENST00000622132.5:c.2785A>C MANE Select	ENSP00000478255.1:p.Arg929=
ENST00000265724.7:c.2785A>C	ENSP00000265724.3:p.Arg929=
ENST00000483831.1:n.343A>C
ENST00000488737.6:n.427A>C
ENST00000496821.5:n.413A>C
ENST00000543898.5:c.2593A>C	ENSP00000444095.1:p.Arg865=
ENST00000622132.4:c.2785A>C	ENSP00000478255.1:p.Arg929=
NM_000927.4:c.2785A>C	NP_000918.2:p.Arg929=
NM_001348944.1:c.2785A>C	NP_001335873.1:p.Arg929=
NM_001348945.1:c.2995A>C	NP_001335874.1:p.Arg999=
NM_001348946.1:c.2785A>C	NP_001335875.1:p.Arg929=
NM_001348946.2:c.2785A>C MANE Select	NP_001335875.1:p.Arg929=
NM_000927.5:c.2785A>C	NP_000918.2:p.Arg929=
NM_001348944.2:c.2785A>C	NP_001335873.1:p.Arg929=
NM_001348945.2:c.2995A>C	NP_001335874.1:p.Arg999=