Canonical Allele Identifier: CA1723621303
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87503896T= , CM000669.2:g.87503896T= GRCh38
NC_000007.13:g.87133212T= , CM000669.1:g.87133212T= GRCh37
NC_000007.12:g.86971148T= NCBI36
NG_011513.1:g.214353A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.*347A= ENSP00000265724.3:n.*347A=
ENST00000622132.5:c.*347A= MANE Select ENSP00000478255.1:n.*347A=
ENST00000265724.7:c.*347A= ENSP00000265724.3:n.*347A=
ENST00000488737.6:n.1832A=
ENST00000543898.5:c.*347A= ENSP00000444095.1:n.*347A=
ENST00000622132.4:c.*347A= ENSP00000478255.1:n.*347A=
NM_000927.4:c.*347A= NP_000918.2:n.*347A=
NM_001348944.1:c.*347A= NP_001335873.1:n.*347A=
NM_001348945.1:c.*347A= NP_001335874.1:n.*347A=
NM_001348946.1:c.*347A= NP_001335875.1:n.*347A=
NM_001348946.2:c.*347A= MANE Select NP_001335875.1:n.*347A=
NM_000927.5:c.*347A= NP_000918.2:n.*347A=
NM_001348944.2:c.*347A= NP_001335873.1:n.*347A=
NM_001348945.2:c.*347A= NP_001335874.1:n.*347A=