Canonical Allele Identifier: CA1723661764
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600828A= , CM000669.2:g.87600828A= GRCh38
NC_000007.13:g.87230144A= , CM000669.1:g.87230144A= GRCh37
NC_000007.12:g.87068080A= NCBI36
NG_011513.1:g.117421T=

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.-80T= ENSP00000265724.3:n.-80T=
ENST00000622132.5:c.-80T= MANE Select ENSP00000478255.1:n.-80T=
ENST00000265724.7:c.-80T= ENSP00000265724.3:n.-80T=
ENST00000416177.1:c.-77-3T= ENSP00000399419.1:n.-77-3T=
ENST00000476862.1:n.567T=
ENST00000543898.5:c.-80T= ENSP00000444095.1:n.-80T=
ENST00000622132.4:c.-80T= ENSP00000478255.1:n.-80T=
NM_000927.4:c.-80T= NP_000918.2:n.-80T=
NM_001348944.1:c.-77-3T= NP_001335873.1:n.-77-3T=
NM_001348945.1:c.134-3T= NP_001335874.1:n.134-3T=
NM_001348946.1:c.-80T= NP_001335875.1:n.-80T=
NM_001348946.2:c.-80T= MANE Select NP_001335875.1:n.-80T=
NM_000927.5:c.-80T= NP_000918.2:n.-80T=
NM_001348944.2:c.-77-3T= NP_001335873.1:n.-77-3T=
NM_001348945.2:c.134-3T= NP_001335874.1:n.134-3T=