Canonical Allele Identifier: CA915945178

Gene: ABCB1

Linked Data

• ClinVar Variation Id: 829317
• ClinVar RCV Id: RCV001029238
• dbSNP Id: rs1584915173
• gnomAD v4: 7-87600863-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600863T>C , CM000669.2:g.87600863T>C	GRCh38
NC_000007.13:g.87230179T>C , CM000669.1:g.87230179T>C	GRCh37
NC_000007.12:g.87068115T>C	NCBI36
NG_011513.1:g.117386A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.-115A>G	ENSP00000265724.3:n.-115A>G
ENST00000622132.5:c.-115A>G MANE Select	ENSP00000478255.1:n.-115A>G
ENST00000265724.7:c.-115A>G	ENSP00000265724.3:n.-115A>G
ENST00000416177.1:c.-77-38A>G	ENSP00000399419.1:n.-77-38A>G
ENST00000476862.1:n.532A>G
ENST00000543898.5:c.-115A>G	ENSP00000444095.1:n.-115A>G
ENST00000622132.4:c.-115A>G	ENSP00000478255.1:n.-115A>G
NM_000927.4:c.-115A>G	NP_000918.2:n.-115A>G
NM_001348944.1:c.-77-38A>G	NP_001335873.1:n.-77-38A>G
NM_001348945.1:c.134-38A>G	NP_001335874.1:n.134-38A>G
NM_001348946.1:c.-115A>G	NP_001335875.1:n.-115A>G
NM_001348946.2:c.-115A>G MANE Select	NP_001335875.1:n.-115A>G
NM_000927.5:c.-115A>G	NP_000918.2:n.-115A>G
NM_001348944.2:c.-77-38A>G	NP_001335873.1:n.-77-38A>G
NM_001348945.2:c.134-38A>G	NP_001335874.1:n.134-38A>G