Canonical Allele Identifier: CA915945179

Gene: ABCB1

Linked Data

• ClinVar Variation Id: 829315
• ClinVar RCV Id: RCV001029236
• dbSNP Id: rs1584915238
• gnomAD v4: 7-87600912-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600912G>A , CM000669.2:g.87600912G>A	GRCh38
NC_000007.13:g.87230228G>A , CM000669.1:g.87230228G>A	GRCh37
NC_000007.12:g.87068164G>A	NCBI36
NG_011513.1:g.117337C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-164C>T	ENSP00000265724.3:n.-164C>T
ENST00000265724.7:c.-164C>T	ENSP00000265724.3:n.-164C>T
ENST00000416177.1:c.-78+61C>T	ENSP00000399419.1:n.-78+61C>T
ENST00000476862.1:n.483C>T
ENST00000543898.5:c.-164C>T	ENSP00000444095.1:n.-164C>T
ENST00000622132.4:c.-164C>T	ENSP00000478255.1:n.-164C>T
NM_000927.4:c.-164C>T	NP_000918.2:n.-164C>T
NM_001348944.1:c.-78+61C>T	NP_001335873.1:n.-78+61C>T
NM_001348945.1:c.133+61C>T	NP_001335874.1:n.133+61C>T
NM_000927.5:c.-164C>T	NP_000918.2:n.-164C>T
NM_001348944.2:c.-78+61C>T	NP_001335873.1:n.-78+61C>T
NM_001348945.2:c.133+61C>T	NP_001335874.1:n.133+61C>T