Canonical Allele Identifier: CA915945184

Gene: ABCB1

Linked Data

• ClinVar Variation Id: 829310
• ClinVar RCV Id: RCV001029231
• dbSNP Id: rs1584915300
• gnomAD v4: 7-87600956-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600956C>T , CM000669.2:g.87600956C>T	GRCh38
NC_000007.13:g.87230272C>T , CM000669.1:g.87230272C>T	GRCh37
NC_000007.12:g.87068208C>T	NCBI36
NG_011513.1:g.117293G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.-208G>A	ENSP00000265724.3:n.-208G>A
ENST00000265724.7:c.-208G>A	ENSP00000265724.3:n.-208G>A
ENST00000416177.1:c.-78+17G>A	ENSP00000399419.1:n.-78+17G>A
ENST00000476862.1:n.439G>A
ENST00000543898.5:c.-208G>A	ENSP00000444095.1:n.-208G>A
ENST00000622132.4:c.-208G>A	ENSP00000478255.1:n.-208G>A
NM_000927.4:c.-208G>A	NP_000918.2:n.-208G>A
NM_001348944.1:c.-78+17G>A	NP_001335873.1:n.-78+17G>A
NM_001348945.1:c.133+17G>A	NP_001335874.1:n.133+17G>A
NM_000927.5:c.-208G>A	NP_000918.2:n.-208G>A
NM_001348944.2:c.-78+17G>A	NP_001335873.1:n.-78+17G>A
NM_001348945.2:c.133+17G>A	NP_001335874.1:n.133+17G>A