Canonical Allele Identifier: CA1104137058
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1160560450
gnomAD v3: 7-87600899-T-A
gnomAD v4: 7-87600899-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600899T>A , CM000669.2:g.87600899T>A GRCh38
NC_000007.13:g.87230215T>A , CM000669.1:g.87230215T>A GRCh37
NC_000007.12:g.87068151T>A NCBI36
NG_011513.1:g.117350A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.-151A>T ENSP00000265724.3:n.-151A>T
ENST00000265724.7:c.-151A>T ENSP00000265724.3:n.-151A>T
ENST00000416177.1:c.-77-74A>T ENSP00000399419.1:n.-77-74A>T
ENST00000476862.1:n.496A>T
ENST00000543898.5:c.-151A>T ENSP00000444095.1:n.-151A>T
ENST00000622132.4:c.-151A>T ENSP00000478255.1:n.-151A>T
NM_000927.4:c.-151A>T NP_000918.2:n.-151A>T
NM_001348944.1:c.-77-74A>T NP_001335873.1:n.-77-74A>T
NM_001348945.1:c.134-74A>T NP_001335874.1:n.134-74A>T
NM_000927.5:c.-151A>T NP_000918.2:n.-151A>T
NM_001348944.2:c.-77-74A>T NP_001335873.1:n.-77-74A>T
NM_001348945.2:c.134-74A>T NP_001335874.1:n.134-74A>T