Canonical Allele Identifier: CA2683610092
Gene: ABCB1 HGNC NCBI

Linked Data

gnomAD v4: 7-87600888-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600888C>A , CM000669.2:g.87600888C>A GRCh38
NC_000007.13:g.87230204C>A , CM000669.1:g.87230204C>A GRCh37
NC_000007.12:g.87068140C>A NCBI36
NG_011513.1:g.117361G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.-140G>T ENSP00000265724.3:n.-140G>T
ENST00000265724.7:c.-140G>T ENSP00000265724.3:n.-140G>T
ENST00000416177.1:c.-77-63G>T ENSP00000399419.1:n.-77-63G>T
ENST00000476862.1:n.507G>T
ENST00000543898.5:c.-140G>T ENSP00000444095.1:n.-140G>T
ENST00000622132.4:c.-140G>T ENSP00000478255.1:n.-140G>T
NM_000927.4:c.-140G>T NP_000918.2:n.-140G>T
NM_001348944.1:c.-77-63G>T NP_001335873.1:n.-77-63G>T
NM_001348945.1:c.134-63G>T NP_001335874.1:n.134-63G>T
NM_001348946.1:c.-140G>T NP_001335875.1:n.-140G>T
NM_000927.5:c.-140G>T NP_000918.2:n.-140G>T
NM_001348944.2:c.-77-63G>T NP_001335873.1:n.-77-63G>T
NM_001348945.2:c.134-63G>T NP_001335874.1:n.134-63G>T