Canonical Allele Identifier: CA1723630258
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1817051402

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87551183_87551186del , CM000669.2:g.87551183_87551186del GRCh38
NC_000007.13:g.87180499_87180502del , CM000669.1:g.87180499_87180502del GRCh37
NC_000007.12:g.87018435_87018438del NCBI36
NG_011513.1:g.167065_167068del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1000-346_1000-343del ENSP00000265724.3:n.1000-346_1000-343del
ENST00000622132.5:c.1000-346_1000-343del MANE Select ENSP00000478255.1:n.1000-346_1000-343del
ENST00000265724.7:c.1000-346_1000-343del ENSP00000265724.3:n.1000-346_1000-343del
ENST00000543898.5:c.808-346_808-343del ENSP00000444095.1:n.808-346_808-343del
ENST00000622132.4:c.1000-346_1000-343del ENSP00000478255.1:n.1000-346_1000-343del
NM_000927.4:c.1000-346_1000-343del NP_000918.2:n.1000-346_1000-343del
NM_001348944.1:c.1000-346_1000-343del NP_001335873.1:n.1000-346_1000-343del
NM_001348945.1:c.1210-346_1210-343del NP_001335874.1:n.1210-346_1210-343del
NM_001348946.1:c.1000-346_1000-343del NP_001335875.1:n.1000-346_1000-343del
NM_001348946.2:c.1000-346_1000-343del MANE Select NP_001335875.1:n.1000-346_1000-343del
NM_000927.5:c.1000-346_1000-343del NP_000918.2:n.1000-346_1000-343del
NM_001348944.2:c.1000-346_1000-343del NP_001335873.1:n.1000-346_1000-343del
NM_001348945.2:c.1210-346_1210-343del NP_001335874.1:n.1210-346_1210-343del