Canonical Allele Identifier: CA368062406

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87179344C>A (hg19) ; chr7:g.87550028C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550028C>A , CM000669.2:g.87550028C>A	GRCh38
NC_000007.13:g.87179344C>A , CM000669.1:g.87179344C>A	GRCh37
NC_000007.12:g.87017280C>A	NCBI36
NG_011513.1:g.168221G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1377G>T	ENSP00000265724.3:p.Arg459Ser
ENST00000622132.5:c.1377G>T MANE Select	ENSP00000478255.1:p.Arg459Ser
ENST00000265724.7:c.1377G>T	ENSP00000265724.3:p.Arg459Ser
ENST00000482527.1:n.131G>T
ENST00000543898.5:c.1185G>T	ENSP00000444095.1:p.Arg395Ser
ENST00000622132.4:c.1377G>T	ENSP00000478255.1:p.Arg459Ser
NM_000927.4:c.1377G>T	NP_000918.2:p.Arg459Ser
NM_001348944.1:c.1377G>T	NP_001335873.1:p.Arg459Ser
NM_001348945.1:c.1587G>T	NP_001335874.1:p.Arg529Ser
NM_001348946.1:c.1377G>T	NP_001335875.1:p.Arg459Ser
NM_001348946.2:c.1377G>T MANE Select	NP_001335875.1:p.Arg459Ser
NM_000927.5:c.1377G>T	NP_000918.2:p.Arg459Ser
NM_001348944.2:c.1377G>T	NP_001335873.1:p.Arg459Ser
NM_001348945.2:c.1587G>T	NP_001335874.1:p.Arg529Ser