Canonical Allele Identifier: CA368044513

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87144695G>C (hg19) ; chr7:g.87515379G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515379G>C , CM000669.2:g.87515379G>C	GRCh38
NC_000007.13:g.87144695G>C , CM000669.1:g.87144695G>C	GRCh37
NC_000007.12:g.86982631G>C	NCBI36
NG_011513.1:g.202870C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3134C>G	ENSP00000265724.3:p.Pro1045Arg
ENST00000622132.5:c.3134C>G MANE Select	ENSP00000478255.1:p.Pro1045Arg
ENST00000265724.7:c.3134C>G	ENSP00000265724.3:p.Pro1045Arg
ENST00000475929.5:n.290C>G
ENST00000488737.6:n.776C>G
ENST00000496821.5:n.762C>G
ENST00000543898.5:c.2942C>G	ENSP00000444095.1:p.Pro981Arg
ENST00000622132.4:c.3134C>G	ENSP00000478255.1:p.Pro1045Arg
NM_000927.4:c.3134C>G	NP_000918.2:p.Pro1045Arg
NM_001348944.1:c.3134C>G	NP_001335873.1:p.Pro1045Arg
NM_001348945.1:c.3344C>G	NP_001335874.1:p.Pro1115Arg
NM_001348946.1:c.3134C>G	NP_001335875.1:p.Pro1045Arg
NM_001348946.2:c.3134C>G MANE Select	NP_001335875.1:p.Pro1045Arg
NM_000927.5:c.3134C>G	NP_000918.2:p.Pro1045Arg
NM_001348944.2:c.3134C>G	NP_001335873.1:p.Pro1045Arg
NM_001348945.2:c.3344C>G	NP_001335874.1:p.Pro1115Arg