Canonical Allele Identifier: CA1723645223

Gene: ABCB1

Linked Data

• dbSNP Id: rs1817623987

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87562885_87562893del , CM000669.2:g.87562885_87562893del	GRCh38
NC_000007.13:g.87192201_87192209del , CM000669.1:g.87192201_87192209del	GRCh37
NC_000007.12:g.87030137_87030145del	NCBI36
NG_011513.1:g.155356_155364del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.703-1506_703-1498del	ENSP00000265724.3:n.703-1506_703-1498del
ENST00000622132.5:c.703-1506_703-1498del MANE Select	ENSP00000478255.1:n.703-1506_703-1498del
ENST00000265724.7:c.703-1506_703-1498del	ENSP00000265724.3:n.703-1506_703-1498del
ENST00000543898.5:c.511-1506_511-1498del	ENSP00000444095.1:n.511-1506_511-1498del
ENST00000622132.4:c.703-1506_703-1498del	ENSP00000478255.1:n.703-1506_703-1498del
NM_000927.4:c.703-1506_703-1498del	NP_000918.2:n.703-1506_703-1498del
NM_001348944.1:c.703-1506_703-1498del	NP_001335873.1:n.703-1506_703-1498del
NM_001348945.1:c.913-1506_913-1498del	NP_001335874.1:n.913-1506_913-1498del
NM_001348946.1:c.703-1506_703-1498del	NP_001335875.1:n.703-1506_703-1498del
NM_001348946.2:c.703-1506_703-1498del MANE Select	NP_001335875.1:n.703-1506_703-1498del
NM_000927.5:c.703-1506_703-1498del	NP_000918.2:n.703-1506_703-1498del
NM_001348944.2:c.703-1506_703-1498del	NP_001335873.1:n.703-1506_703-1498del
NM_001348945.2:c.913-1506_913-1498del	NP_001335874.1:n.913-1506_913-1498del