Canonical Allele Identifier: CA1723632230

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816043837

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531261_87531272del , CM000669.2:g.87531261_87531272del	GRCh38
NC_000007.13:g.87160577_87160588del , CM000669.1:g.87160577_87160588del	GRCh37
NC_000007.12:g.86998513_86998524del	NCBI36
NG_011513.1:g.186978_186989del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2685+23_2685+34del	ENSP00000265724.3:n.2685+23_2685+34del
ENST00000622132.5:c.2685+23_2685+34del MANE Select	ENSP00000478255.1:n.2685+23_2685+34del
ENST00000265724.7:c.2685+23_2685+34del	ENSP00000265724.3:n.2685+23_2685+34del
ENST00000488737.6:n.327+23_327+34del
ENST00000496821.5:n.313+23_313+34del
ENST00000543898.5:c.2493+23_2493+34del	ENSP00000444095.1:n.2493+23_2493+34del
ENST00000622132.4:c.2685+23_2685+34del	ENSP00000478255.1:n.2685+23_2685+34del
NM_000927.4:c.2685+23_2685+34del	NP_000918.2:n.2685+23_2685+34del
NM_001348944.1:c.2685+23_2685+34del	NP_001335873.1:n.2685+23_2685+34del
NM_001348945.1:c.2895+23_2895+34del	NP_001335874.1:n.2895+23_2895+34del
NM_001348946.1:c.2685+23_2685+34del	NP_001335875.1:n.2685+23_2685+34del
NM_001348946.2:c.2685+23_2685+34del MANE Select	NP_001335875.1:n.2685+23_2685+34del
NM_000927.5:c.2685+23_2685+34del	NP_000918.2:n.2685+23_2685+34del
NM_001348944.2:c.2685+23_2685+34del	NP_001335873.1:n.2685+23_2685+34del
NM_001348945.2:c.2895+23_2895+34del	NP_001335874.1:n.2895+23_2895+34del