Canonical Allele Identifier: CA162123156

Gene: ABCB1

Linked Data

• dbSNP Id: rs34885273
• MyVariant Identifiers: chr7:g.87179668_87179669insT (hg19) ; chr7:g.87550352_87550353insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550352_87550353insT , CM000669.2:g.87550352_87550353insT	GRCh38
NC_000007.13:g.87179668_87179669insT , CM000669.1:g.87179668_87179669insT	GRCh37
NC_000007.12:g.87017604_87017605insT	NCBI36
NG_011513.1:g.167896_167897insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1225-57_1225-56insA	ENSP00000265724.3:n.1225-57_1225-56insA
ENST00000622132.5:c.1225-57_1225-56insA MANE Select	ENSP00000478255.1:n.1225-57_1225-56insA
ENST00000265724.7:c.1225-57_1225-56insA	ENSP00000265724.3:n.1225-57_1225-56insA
ENST00000543898.5:c.1033-57_1033-56insA	ENSP00000444095.1:n.1033-57_1033-56insA
ENST00000622132.4:c.1225-57_1225-56insA	ENSP00000478255.1:n.1225-57_1225-56insA
NM_000927.4:c.1225-57_1225-56insA	NP_000918.2:n.1225-57_1225-56insA
NM_001348944.1:c.1225-57_1225-56insA	NP_001335873.1:n.1225-57_1225-56insA
NM_001348945.1:c.1435-57_1435-56insA	NP_001335874.1:n.1435-57_1435-56insA
NM_001348946.1:c.1225-57_1225-56insA	NP_001335875.1:n.1225-57_1225-56insA
NM_001348946.2:c.1225-57_1225-56insA MANE Select	NP_001335875.1:n.1225-57_1225-56insA
NM_000927.5:c.1225-57_1225-56insA	NP_000918.2:n.1225-57_1225-56insA
NM_001348944.2:c.1225-57_1225-56insA	NP_001335873.1:n.1225-57_1225-56insA
NM_001348945.2:c.1435-57_1435-56insA	NP_001335874.1:n.1435-57_1435-56insA