Canonical Allele Identifier: CA368049935

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87150098G>C (hg19) ; chr7:g.87520782G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520782G>C , CM000669.2:g.87520782G>C	GRCh38
NC_000007.13:g.87150098G>C , CM000669.1:g.87150098G>C	GRCh37
NC_000007.12:g.86988034G>C	NCBI36
NG_011513.1:g.197467C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2780C>G	ENSP00000265724.3:p.Pro927Arg
ENST00000622132.5:c.2780C>G MANE Select	ENSP00000478255.1:p.Pro927Arg
ENST00000265724.7:c.2780C>G	ENSP00000265724.3:p.Pro927Arg
ENST00000483831.1:n.338C>G
ENST00000488737.6:n.422C>G
ENST00000496821.5:n.408C>G
ENST00000543898.5:c.2588C>G	ENSP00000444095.1:p.Pro863Arg
ENST00000622132.4:c.2780C>G	ENSP00000478255.1:p.Pro927Arg
NM_000927.4:c.2780C>G	NP_000918.2:p.Pro927Arg
NM_001348944.1:c.2780C>G	NP_001335873.1:p.Pro927Arg
NM_001348945.1:c.2990C>G	NP_001335874.1:p.Pro997Arg
NM_001348946.1:c.2780C>G	NP_001335875.1:p.Pro927Arg
NM_001348946.2:c.2780C>G MANE Select	NP_001335875.1:p.Pro927Arg
NM_000927.5:c.2780C>G	NP_000918.2:p.Pro927Arg
NM_001348944.2:c.2780C>G	NP_001335873.1:p.Pro927Arg
NM_001348945.2:c.2990C>G	NP_001335874.1:p.Pro997Arg