Canonical Allele Identifier: CA1723661802
Gene: ABCB1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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