Canonical Allele Identifier: CA915945157

Gene: ABCB1

Linked Data

• ClinVar Variation Id: 829323
• ClinVar RCV Id: RCV001029244
• dbSNP Id: rs1584914521
• gnomAD v4: 7-87600234-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600234G>T , CM000669.2:g.87600234G>T	GRCh38
NC_000007.13:g.87229550G>T , CM000669.1:g.87229550G>T	GRCh37
NC_000007.12:g.87067486G>T	NCBI36
NG_011513.1:g.118015C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.-6-44C>A	ENSP00000265724.3:n.-6-44C>A
ENST00000622132.5:c.-6-44C>A MANE Select	ENSP00000478255.1:n.-6-44C>A
ENST00000265724.7:c.-6-44C>A	ENSP00000265724.3:n.-6-44C>A
ENST00000416177.1:c.-6-44C>A	ENSP00000399419.1:n.-6-44C>A
ENST00000543898.5:c.-6-44C>A	ENSP00000444095.1:n.-6-44C>A
ENST00000622132.4:c.-6-44C>A	ENSP00000478255.1:n.-6-44C>A
NM_000927.4:c.-6-44C>A	NP_000918.2:n.-6-44C>A
NM_001348944.1:c.-6-44C>A	NP_001335873.1:n.-6-44C>A
NM_001348945.1:c.205-44C>A	NP_001335874.1:n.205-44C>A
NM_001348946.1:c.-6-44C>A	NP_001335875.1:n.-6-44C>A
NM_001348946.2:c.-6-44C>A MANE Select	NP_001335875.1:n.-6-44C>A
NM_000927.5:c.-6-44C>A	NP_000918.2:n.-6-44C>A
NM_001348944.2:c.-6-44C>A	NP_001335873.1:n.-6-44C>A
NM_001348945.2:c.205-44C>A	NP_001335874.1:n.205-44C>A