Canonical Allele Identifier: CA915945260

Gene: ABCB1

Linked Data

• ClinVar Variation Id: 829470
• ClinVar RCV Id: RCV001029392
• dbSNP Id: rs1584871672

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550311G>A , CM000669.2:g.87550311G>A	GRCh38
NC_000007.13:g.87179627G>A , CM000669.1:g.87179627G>A	GRCh37
NC_000007.12:g.87017563G>A	NCBI36
NG_011513.1:g.167938C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1225-15C>T	ENSP00000265724.3:n.1225-15C>T
ENST00000622132.5:c.1225-15C>T MANE Select	ENSP00000478255.1:n.1225-15C>T
ENST00000265724.7:c.1225-15C>T	ENSP00000265724.3:n.1225-15C>T
ENST00000543898.5:c.1033-15C>T	ENSP00000444095.1:n.1033-15C>T
ENST00000622132.4:c.1225-15C>T	ENSP00000478255.1:n.1225-15C>T
NM_000927.4:c.1225-15C>T	NP_000918.2:n.1225-15C>T
NM_001348944.1:c.1225-15C>T	NP_001335873.1:n.1225-15C>T
NM_001348945.1:c.1435-15C>T	NP_001335874.1:n.1435-15C>T
NM_001348946.1:c.1225-15C>T	NP_001335875.1:n.1225-15C>T
NM_001348946.2:c.1225-15C>T MANE Select	NP_001335875.1:n.1225-15C>T
NM_000927.5:c.1225-15C>T	NP_000918.2:n.1225-15C>T
NM_001348944.2:c.1225-15C>T	NP_001335873.1:n.1225-15C>T
NM_001348945.2:c.1435-15C>T	NP_001335874.1:n.1435-15C>T