Canonical Allele Identifier: CA368094317

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87229476C>G (hg19) ; chr7:g.87600160C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600160C>G , CM000669.2:g.87600160C>G	GRCh38
NC_000007.13:g.87229476C>G , CM000669.1:g.87229476C>G	GRCh37
NC_000007.12:g.87067412C>G	NCBI36
NG_011513.1:g.118089G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.25G>C	ENSP00000265724.3:p.Gly9Arg
ENST00000622132.5:c.25G>C MANE Select	ENSP00000478255.1:p.Gly9Arg
ENST00000265724.7:c.25G>C	ENSP00000265724.3:p.Gly9Arg
ENST00000416177.1:c.25G>C	ENSP00000399419.1:p.Gly9Arg
ENST00000543898.5:c.25G>C	ENSP00000444095.1:p.Gly9Arg
ENST00000622132.4:c.25G>C	ENSP00000478255.1:p.Gly9Arg
NM_000927.4:c.25G>C	NP_000918.2:p.Gly9Arg
NM_001348944.1:c.25G>C	NP_001335873.1:p.Gly9Arg
NM_001348945.1:c.235G>C	NP_001335874.1:p.Gly79Arg
NM_001348946.1:c.25G>C	NP_001335875.1:p.Gly9Arg
NM_001348946.2:c.25G>C MANE Select	NP_001335875.1:p.Gly9Arg
NM_000927.5:c.25G>C	NP_000918.2:p.Gly9Arg
NM_001348944.2:c.25G>C	NP_001335873.1:p.Gly9Arg
NM_001348945.2:c.235G>C	NP_001335874.1:p.Gly79Arg