Canonical Allele Identifier: CA1104136789
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1819379304

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600029_87600030del , CM000669.2:g.87600029_87600030del GRCh38
NC_000007.13:g.87229345_87229346del , CM000669.1:g.87229345_87229346del GRCh37
NC_000007.12:g.87067281_87067282del NCBI36
NG_011513.1:g.118219_118220del

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.68+87_68+88del ENSP00000265724.3:n.68+87_68+88del
ENST00000622132.5:c.68+87_68+88del MANE Select ENSP00000478255.1:n.68+87_68+88del
ENST00000265724.7:c.68+87_68+88del ENSP00000265724.3:n.68+87_68+88del
ENST00000416177.1:c.68+87_68+88del ENSP00000399419.1:n.68+87_68+88del
ENST00000543898.5:c.68+87_68+88del ENSP00000444095.1:n.68+87_68+88del
ENST00000622132.4:c.68+87_68+88del ENSP00000478255.1:n.68+87_68+88del
NM_000927.4:c.68+87_68+88del NP_000918.2:n.68+87_68+88del
NM_001348944.1:c.68+87_68+88del NP_001335873.1:n.68+87_68+88del
NM_001348945.1:c.278+87_278+88del NP_001335874.1:n.278+87_278+88del
NM_001348946.1:c.68+87_68+88del NP_001335875.1:n.68+87_68+88del
NM_001348946.2:c.68+87_68+88del MANE Select NP_001335875.1:n.68+87_68+88del
NM_000927.5:c.68+87_68+88del NP_000918.2:n.68+87_68+88del
NM_001348944.2:c.68+87_68+88del NP_001335873.1:n.68+87_68+88del
NM_001348945.2:c.278+87_278+88del NP_001335874.1:n.278+87_278+88del