Canonical Allele Identifier: CA162112866

Gene: ABCB1

Linked Data

• dbSNP Id: rs776226968
• MyVariant Identifiers: chr7:g.87165006_87165009del (hg19) ; chr7:g.87535690_87535693del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87535693_87535696del , CM000669.2:g.87535693_87535696del	GRCh38
NC_000007.13:g.87165009_87165012del , CM000669.1:g.87165009_87165012del	GRCh37
NC_000007.12:g.87002945_87002948del	NCBI36
NG_011513.1:g.182556_182559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2481+765_2481+768del	ENSP00000265724.3:n.2481+765_2481+768del
ENST00000622132.5:c.2481+765_2481+768del MANE Select	ENSP00000478255.1:n.2481+765_2481+768del
ENST00000265724.7:c.2481+765_2481+768del	ENSP00000265724.3:n.2481+765_2481+768del
ENST00000496821.5:n.109+765_109+768del
ENST00000543898.5:c.2289+765_2289+768del	ENSP00000444095.1:n.2289+765_2289+768del
ENST00000622132.4:c.2481+765_2481+768del	ENSP00000478255.1:n.2481+765_2481+768del
NM_000927.4:c.2481+765_2481+768del	NP_000918.2:n.2481+765_2481+768del
NM_001348944.1:c.2481+765_2481+768del	NP_001335873.1:n.2481+765_2481+768del
NM_001348945.1:c.2691+765_2691+768del	NP_001335874.1:n.2691+765_2691+768del
NM_001348946.1:c.2481+765_2481+768del	NP_001335875.1:n.2481+765_2481+768del
NM_001348946.2:c.2481+765_2481+768del MANE Select	NP_001335875.1:n.2481+765_2481+768del
NM_000927.5:c.2481+765_2481+768del	NP_000918.2:n.2481+765_2481+768del
NM_001348944.2:c.2481+765_2481+768del	NP_001335873.1:n.2481+765_2481+768del
NM_001348945.2:c.2691+765_2691+768del	NP_001335874.1:n.2691+765_2691+768del