Canonical Allele Identifier: CA843382939

Gene: ABCB1

Linked Data

• dbSNP Id: rs1278465915
• gnomAD v3: 7-87540084-G-GT
• gnomAD v4: 7-87540084-G-GT
• MyVariant Identifiers: chr7:g.87169400_87169401insT (hg19) ; chr7:g.87540084_87540085insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87540090dup , CM000669.2:g.87540090dup	GRCh38
NC_000007.13:g.87169406dup , CM000669.1:g.87169406dup	GRCh37
NC_000007.12:g.87007342dup	NCBI36
NG_011513.1:g.178164dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2320-740dup	ENSP00000265724.3:n.2320-740dup
ENST00000622132.5:c.2320-740dup MANE Select	ENSP00000478255.1:n.2320-740dup
ENST00000265724.7:c.2320-740dup	ENSP00000265724.3:n.2320-740dup
ENST00000543898.5:c.2128-740dup	ENSP00000444095.1:n.2128-740dup
ENST00000622132.4:c.2320-740dup	ENSP00000478255.1:n.2320-740dup
NM_000927.4:c.2320-740dup	NP_000918.2:n.2320-740dup
NM_001348944.1:c.2320-740dup	NP_001335873.1:n.2320-740dup
NM_001348945.1:c.2530-740dup	NP_001335874.1:n.2530-740dup
NM_001348946.1:c.2320-740dup	NP_001335875.1:n.2320-740dup
NM_001348946.2:c.2320-740dup MANE Select	NP_001335875.1:n.2320-740dup
NM_000927.5:c.2320-740dup	NP_000918.2:n.2320-740dup
NM_001348944.2:c.2320-740dup	NP_001335873.1:n.2320-740dup
NM_001348945.2:c.2530-740dup	NP_001335874.1:n.2530-740dup