Canonical Allele Identifier: CA1104136901
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1819396598

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600343_87600344insCTGCACAGGAAAGCCCCTGCAGTGCCCATCGCGCCCAGCTGCTCTGGCCGCGATGGGCACTGCA , CM000669.2:g.87600343_87600344insCTGCACAGGAAAGCCCCTGCAGTGCCCATCGCGCCCAGCTGCTCTGGCCGCGATGGGCACTGCA GRCh38
NC_000007.13:g.87229659_87229660insCTGCACAGGAAAGCCCCTGCAGTGCCCATCGCGCCCAGCTGCTCTGGCCGCGATGGGCACTGCA , CM000669.1:g.87229659_87229660insCTGCACAGGAAAGCCCCTGCAGTGCCCATCGCGCCCAGCTGCTCTGGCCGCGATGGGCACTGCA GRCh37
NC_000007.12:g.87067595_87067596insCTGCACAGGAAAGCCCCTGCAGTGCCCATCGCGCCCAGCTGCTCTGGCCGCGATGGGCACTGCA NCBI36
NG_011513.1:g.117936_117937insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG ENSP00000265724.3:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTC...
ENST00000622132.5:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG MANE Select ENSP00000478255.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTC...
ENST00000265724.7:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG ENSP00000265724.3:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTC...
ENST00000416177.1:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG ENSP00000399419.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTC...
ENST00000543898.5:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG ENSP00000444095.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTC...
ENST00000622132.4:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG ENSP00000478255.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTC...
NM_000927.4:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_000918.2:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGC...
NM_001348944.1:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_001335873.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTG...
NM_001348945.1:c.205-123_205-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_001335874.1:n.205-123_205-122insCGCGATGGGCACTGCAGGGGCTTTCC...
NM_001348946.1:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_001335875.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTG...
NM_001348946.2:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG MANE Select NP_001335875.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTG...
NM_000927.5:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_000918.2:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGC...
NM_001348944.2:c.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_001335873.1:n.-6-123_-6-122insCGCGATGGGCACTGCAGGGGCTTTCCTG...
NM_001348945.2:c.205-123_205-122insCGCGATGGGCACTGCAGGGGCTTTCCTGTGCAGTGCAGTGCCCATCGCGGCCAGAGCAGCTGGG NP_001335874.1:n.205-123_205-122insCGCGATGGGCACTGCAGGGGCTTTCC...