Canonical Allele Identifier: CA1723630939
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1816002624

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530793_87530794dup , CM000669.2:g.87530793_87530794dup GRCh38
NC_000007.13:g.87160109_87160110dup , CM000669.1:g.87160109_87160110dup GRCh37
NC_000007.12:g.86998045_86998046dup NCBI36
NG_011513.1:g.187456_187457dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+501_2685+502dup ENSP00000265724.3:n.2685+501_2685+502dup
ENST00000622132.5:c.2685+501_2685+502dup MANE Select ENSP00000478255.1:n.2685+501_2685+502dup
ENST00000265724.7:c.2685+501_2685+502dup ENSP00000265724.3:n.2685+501_2685+502dup
ENST00000488737.6:n.327+501_327+502dup
ENST00000496821.5:n.313+501_313+502dup
ENST00000543898.5:c.2493+501_2493+502dup ENSP00000444095.1:n.2493+501_2493+502dup
ENST00000622132.4:c.2685+501_2685+502dup ENSP00000478255.1:n.2685+501_2685+502dup
NM_000927.4:c.2685+501_2685+502dup NP_000918.2:n.2685+501_2685+502dup
NM_001348944.1:c.2685+501_2685+502dup NP_001335873.1:n.2685+501_2685+502dup
NM_001348945.1:c.2895+501_2895+502dup NP_001335874.1:n.2895+501_2895+502dup
NM_001348946.1:c.2685+501_2685+502dup NP_001335875.1:n.2685+501_2685+502dup
NM_001348946.2:c.2685+501_2685+502dup MANE Select NP_001335875.1:n.2685+501_2685+502dup
NM_000927.5:c.2685+501_2685+502dup NP_000918.2:n.2685+501_2685+502dup
NM_001348944.2:c.2685+501_2685+502dup NP_001335873.1:n.2685+501_2685+502dup
NM_001348945.2:c.2895+501_2895+502dup NP_001335874.1:n.2895+501_2895+502dup