Canonical Allele Identifier: CA368062916

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87179605T>G (hg19) ; chr7:g.87550289T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550289T>G , CM000669.2:g.87550289T>G	GRCh38
NC_000007.13:g.87179605T>G , CM000669.1:g.87179605T>G	GRCh37
NC_000007.12:g.87017541T>G	NCBI36
NG_011513.1:g.167960A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1232A>C	ENSP00000265724.3:p.Lys411Thr
ENST00000622132.5:c.1232A>C MANE Select	ENSP00000478255.1:p.Lys411Thr
ENST00000265724.7:c.1232A>C	ENSP00000265724.3:p.Lys411Thr
ENST00000543898.5:c.1040A>C	ENSP00000444095.1:p.Lys347Thr
ENST00000622132.4:c.1232A>C	ENSP00000478255.1:p.Lys411Thr
NM_000927.4:c.1232A>C	NP_000918.2:p.Lys411Thr
NM_001348944.1:c.1232A>C	NP_001335873.1:p.Lys411Thr
NM_001348945.1:c.1442A>C	NP_001335874.1:p.Lys481Thr
NM_001348946.1:c.1232A>C	NP_001335875.1:p.Lys411Thr
NM_001348946.2:c.1232A>C MANE Select	NP_001335875.1:p.Lys411Thr
NM_000927.5:c.1232A>C	NP_000918.2:p.Lys411Thr
NM_001348944.2:c.1232A>C	NP_001335873.1:p.Lys411Thr
NM_001348945.2:c.1442A>C	NP_001335874.1:p.Lys481Thr