Canonical Allele Identifier: CA456372214

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87195542A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87566226A>G , CM000669.2:g.87566226A>G	GRCh38
NC_000007.13:g.87195542A>G , CM000669.1:g.87195542A>G	GRCh37
NC_000007.12:g.87033478A>G	NCBI36
NG_011513.1:g.152023T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.546T>C	ENSP00000265724.3:p.Ile182=
ENST00000622132.5:c.546T>C MANE Select	ENSP00000478255.1:p.Ile182=
ENST00000265724.7:c.546T>C	ENSP00000265724.3:p.Ile182=
ENST00000543898.5:c.354T>C	ENSP00000444095.1:p.Ile118=
ENST00000622132.4:c.546T>C	ENSP00000478255.1:p.Ile182=
NM_000927.4:c.546T>C	NP_000918.2:p.Ile182=
NM_001348944.1:c.546T>C	NP_001335873.1:p.Ile182=
NM_001348945.1:c.756T>C	NP_001335874.1:p.Ile252=
NM_001348946.1:c.546T>C	NP_001335875.1:p.Ile182=
NM_001348946.2:c.546T>C MANE Select	NP_001335875.1:p.Ile182=
NM_000927.5:c.546T>C	NP_000918.2:p.Ile182=
NM_001348944.2:c.546T>C	NP_001335873.1:p.Ile182=
NM_001348945.2:c.756T>C	NP_001335874.1:p.Ile252=