Canonical Allele Identifier: CA575861961
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1456546076

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530931_87530933del , CM000669.2:g.87530931_87530933del GRCh38
NC_000007.13:g.87160247_87160249del , CM000669.1:g.87160247_87160249del GRCh37
NC_000007.12:g.86998183_86998185del NCBI36
NG_011513.1:g.187319_187321del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+364_2685+366del ENSP00000265724.3:n.2685+364_2685+366del
ENST00000622132.5:c.2685+364_2685+366del MANE Select ENSP00000478255.1:n.2685+364_2685+366del
ENST00000265724.7:c.2685+364_2685+366del ENSP00000265724.3:n.2685+364_2685+366del
ENST00000488737.6:n.327+364_327+366del
ENST00000496821.5:n.313+364_313+366del
ENST00000543898.5:c.2493+364_2493+366del ENSP00000444095.1:n.2493+364_2493+366del
ENST00000622132.4:c.2685+364_2685+366del ENSP00000478255.1:n.2685+364_2685+366del
NM_000927.4:c.2685+364_2685+366del NP_000918.2:n.2685+364_2685+366del
NM_001348944.1:c.2685+364_2685+366del NP_001335873.1:n.2685+364_2685+366del
NM_001348945.1:c.2895+364_2895+366del NP_001335874.1:n.2895+364_2895+366del
NM_001348946.1:c.2685+364_2685+366del NP_001335875.1:n.2685+364_2685+366del
NM_001348946.2:c.2685+364_2685+366del MANE Select NP_001335875.1:n.2685+364_2685+366del
NM_000927.5:c.2685+364_2685+366del NP_000918.2:n.2685+364_2685+366del
NM_001348944.2:c.2685+364_2685+366del NP_001335873.1:n.2685+364_2685+366del
NM_001348945.2:c.2895+364_2895+366del NP_001335874.1:n.2895+364_2895+366del