Canonical Allele Identifier: CA843389783

Gene: ABCB1

Linked Data

• dbSNP Id: rs1170760104
• MyVariant Identifiers: chr7:g.87180712del (hg19) ; chr7:g.87551396del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87551397del , CM000669.2:g.87551397del	GRCh38
NC_000007.13:g.87180713del , CM000669.1:g.87180713del	GRCh37
NC_000007.12:g.87018649del	NCBI36
NG_011513.1:g.166853del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1000-558del	ENSP00000265724.3:n.1000-558del
ENST00000622132.5:c.1000-558del MANE Select	ENSP00000478255.1:n.1000-558del
ENST00000265724.7:c.1000-558del	ENSP00000265724.3:n.1000-558del
ENST00000543898.5:c.808-558del	ENSP00000444095.1:n.808-558del
ENST00000622132.4:c.1000-558del	ENSP00000478255.1:n.1000-558del
NM_000927.4:c.1000-558del	NP_000918.2:n.1000-558del
NM_001348944.1:c.1000-558del	NP_001335873.1:n.1000-558del
NM_001348945.1:c.1210-558del	NP_001335874.1:n.1210-558del
NM_001348946.1:c.1000-558del	NP_001335875.1:n.1000-558del
NM_001348946.2:c.1000-558del MANE Select	NP_001335875.1:n.1000-558del
NM_000927.5:c.1000-558del	NP_000918.2:n.1000-558del
NM_001348944.2:c.1000-558del	NP_001335873.1:n.1000-558del
NM_001348945.2:c.1210-558del	NP_001335874.1:n.1210-558del