Canonical Allele Identifier: CA162116372

Gene: ABCB1

Linked Data

• dbSNP Id: rs758671714
• gnomAD v3: 7-87541679-A-AT
• gnomAD v4: 7-87541679-A-AT
• MyVariant Identifiers: chr7:g.87170995_87170996insT (hg19) ; chr7:g.87541679_87541680insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87541685dup , CM000669.2:g.87541685dup	GRCh38
NC_000007.13:g.87171001dup , CM000669.1:g.87171001dup	GRCh37
NC_000007.12:g.87008937dup	NCBI36
NG_011513.1:g.176569dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2212-216dup	ENSP00000265724.3:n.2212-216dup
ENST00000622132.5:c.2212-216dup MANE Select	ENSP00000478255.1:n.2212-216dup
ENST00000265724.7:c.2212-216dup	ENSP00000265724.3:n.2212-216dup
ENST00000543898.5:c.2020-216dup	ENSP00000444095.1:n.2020-216dup
ENST00000622132.4:c.2212-216dup	ENSP00000478255.1:n.2212-216dup
NM_000927.4:c.2212-216dup	NP_000918.2:n.2212-216dup
NM_001348944.1:c.2212-216dup	NP_001335873.1:n.2212-216dup
NM_001348945.1:c.2422-216dup	NP_001335874.1:n.2422-216dup
NM_001348946.1:c.2212-216dup	NP_001335875.1:n.2212-216dup
NM_001348946.2:c.2212-216dup MANE Select	NP_001335875.1:n.2212-216dup
NM_000927.5:c.2212-216dup	NP_000918.2:n.2212-216dup
NM_001348944.2:c.2212-216dup	NP_001335873.1:n.2212-216dup
NM_001348945.2:c.2422-216dup	NP_001335874.1:n.2422-216dup