Canonical Allele Identifier: CA2683610089

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87600882-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600882A>G , CM000669.2:g.87600882A>G	GRCh38
NC_000007.13:g.87230198A>G , CM000669.1:g.87230198A>G	GRCh37
NC_000007.12:g.87068134A>G	NCBI36
NG_011513.1:g.117367T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-134T>C	ENSP00000265724.3:n.-134T>C
ENST00000622132.5:c.-134T>C MANE Select	ENSP00000478255.1:n.-134T>C
ENST00000265724.7:c.-134T>C	ENSP00000265724.3:n.-134T>C
ENST00000416177.1:c.-77-57T>C	ENSP00000399419.1:n.-77-57T>C
ENST00000476862.1:n.513T>C
ENST00000543898.5:c.-134T>C	ENSP00000444095.1:n.-134T>C
ENST00000622132.4:c.-134T>C	ENSP00000478255.1:n.-134T>C
NM_000927.4:c.-134T>C	NP_000918.2:n.-134T>C
NM_001348944.1:c.-77-57T>C	NP_001335873.1:n.-77-57T>C
NM_001348945.1:c.134-57T>C	NP_001335874.1:n.134-57T>C
NM_001348946.1:c.-134T>C	NP_001335875.1:n.-134T>C
NM_001348946.2:c.-134T>C MANE Select	NP_001335875.1:n.-134T>C
NM_000927.5:c.-134T>C	NP_000918.2:n.-134T>C
NM_001348944.2:c.-77-57T>C	NP_001335873.1:n.-77-57T>C
NM_001348945.2:c.134-57T>C	NP_001335874.1:n.134-57T>C