Canonical Allele Identifier: CA4328016
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs775305519

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87531505del , CM000669.2:g.87531505del GRCh38
NC_000007.13:g.87160821del , CM000669.1:g.87160821del GRCh37
NC_000007.12:g.86998757del NCBI36
NG_011513.1:g.186747del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2482-5del ENSP00000265724.3:n.2482-5del
ENST00000622132.5:c.2482-5del MANE Select ENSP00000478255.1:n.2482-5del
ENST00000265724.7:c.2482-5del ENSP00000265724.3:n.2482-5del
ENST00000488737.6:n.124-5del
ENST00000496821.5:n.110-5del
ENST00000543898.5:c.2290-5del ENSP00000444095.1:n.2290-5del
ENST00000622132.4:c.2482-5del ENSP00000478255.1:n.2482-5del
NM_000927.4:c.2482-5del NP_000918.2:n.2482-5del
NM_001348944.1:c.2482-5del NP_001335873.1:n.2482-5del
NM_001348945.1:c.2692-5del NP_001335874.1:n.2692-5del
NM_001348946.1:c.2482-5del NP_001335875.1:n.2482-5del
NM_001348946.2:c.2482-5del MANE Select NP_001335875.1:n.2482-5del
NM_000927.5:c.2482-5del NP_000918.2:n.2482-5del
NM_001348944.2:c.2482-5del NP_001335873.1:n.2482-5del
NM_001348945.2:c.2692-5del NP_001335874.1:n.2692-5del