Canonical Allele Identifier: CA368090389

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87195436T>C (hg19) ; chr7:g.87566120T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87566120T>C , CM000669.2:g.87566120T>C	GRCh38
NC_000007.13:g.87195436T>C , CM000669.1:g.87195436T>C	GRCh37
NC_000007.12:g.87033372T>C	NCBI36
NG_011513.1:g.152129A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.652A>G	ENSP00000265724.3:p.Ile218Val
ENST00000622132.5:c.652A>G MANE Select	ENSP00000478255.1:p.Ile218Val
ENST00000265724.7:c.652A>G	ENSP00000265724.3:p.Ile218Val
ENST00000543898.5:c.460A>G	ENSP00000444095.1:p.Ile154Val
ENST00000622132.4:c.652A>G	ENSP00000478255.1:p.Ile218Val
NM_000927.4:c.652A>G	NP_000918.2:p.Ile218Val
NM_001348944.1:c.652A>G	NP_001335873.1:p.Ile218Val
NM_001348945.1:c.862A>G	NP_001335874.1:p.Ile288Val
NM_001348946.1:c.652A>G	NP_001335875.1:p.Ile218Val
NM_001348946.2:c.652A>G MANE Select	NP_001335875.1:p.Ile218Val
NM_000927.5:c.652A>G	NP_000918.2:p.Ile218Val
NM_001348944.2:c.652A>G	NP_001335873.1:p.Ile218Val
NM_001348945.2:c.862A>G	NP_001335874.1:p.Ile288Val