Canonical Allele Identifier: CA1104138151
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1256115733

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87562775_87562780del , CM000669.2:g.87562775_87562780del GRCh38
NC_000007.13:g.87192091_87192096del , CM000669.1:g.87192091_87192096del GRCh37
NC_000007.12:g.87030027_87030032del NCBI36
NG_011513.1:g.155480_155485del

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.703-1382_703-1377del ENSP00000265724.3:n.703-1382_703-1377del
ENST00000622132.5:c.703-1382_703-1377del MANE Select ENSP00000478255.1:n.703-1382_703-1377del
ENST00000265724.7:c.703-1382_703-1377del ENSP00000265724.3:n.703-1382_703-1377del
ENST00000543898.5:c.511-1382_511-1377del ENSP00000444095.1:n.511-1382_511-1377del
ENST00000622132.4:c.703-1382_703-1377del ENSP00000478255.1:n.703-1382_703-1377del
NM_000927.4:c.703-1382_703-1377del NP_000918.2:n.703-1382_703-1377del
NM_001348944.1:c.703-1382_703-1377del NP_001335873.1:n.703-1382_703-1377del
NM_001348945.1:c.913-1382_913-1377del NP_001335874.1:n.913-1382_913-1377del
NM_001348946.1:c.703-1382_703-1377del NP_001335875.1:n.703-1382_703-1377del
NM_001348946.2:c.703-1382_703-1377del MANE Select NP_001335875.1:n.703-1382_703-1377del
NM_000927.5:c.703-1382_703-1377del NP_000918.2:n.703-1382_703-1377del
NM_001348944.2:c.703-1382_703-1377del NP_001335873.1:n.703-1382_703-1377del
NM_001348945.2:c.913-1382_913-1377del NP_001335874.1:n.913-1382_913-1377del