Canonical Allele Identifier: CA1723639527

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816471292

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87540132_87540144del , CM000669.2:g.87540132_87540144del	GRCh38
NC_000007.13:g.87169448_87169460del , CM000669.1:g.87169448_87169460del	GRCh37
NC_000007.12:g.87007384_87007396del	NCBI36
NG_011513.1:g.178106_178118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2320-798_2320-786del	ENSP00000265724.3:n.2320-798_2320-786del
ENST00000622132.5:c.2320-798_2320-786del MANE Select	ENSP00000478255.1:n.2320-798_2320-786del
ENST00000265724.7:c.2320-798_2320-786del	ENSP00000265724.3:n.2320-798_2320-786del
ENST00000543898.5:c.2128-798_2128-786del	ENSP00000444095.1:n.2128-798_2128-786del
ENST00000622132.4:c.2320-798_2320-786del	ENSP00000478255.1:n.2320-798_2320-786del
NM_000927.4:c.2320-798_2320-786del	NP_000918.2:n.2320-798_2320-786del
NM_001348944.1:c.2320-798_2320-786del	NP_001335873.1:n.2320-798_2320-786del
NM_001348945.1:c.2530-798_2530-786del	NP_001335874.1:n.2530-798_2530-786del
NM_001348946.1:c.2320-798_2320-786del	NP_001335875.1:n.2320-798_2320-786del
NM_001348946.2:c.2320-798_2320-786del MANE Select	NP_001335875.1:n.2320-798_2320-786del
NM_000927.5:c.2320-798_2320-786del	NP_000918.2:n.2320-798_2320-786del
NM_001348944.2:c.2320-798_2320-786del	NP_001335873.1:n.2320-798_2320-786del
NM_001348945.2:c.2530-798_2530-786del	NP_001335874.1:n.2530-798_2530-786del