Canonical Allele Identifier: CA162107545

Gene: ABCB1

Linked Data

• dbSNP Id: rs199705785
• gnomAD v2: 7-87152064-C-CT
• gnomAD v3: 7-87522748-C-CT
• gnomAD v4: 7-87522748-C-CT
• MyVariant Identifiers: chr7:g.87152065_87152066insT (hg19) ; chr7:g.87152064_87152065insT (hg19) ; chr7:g.87522749_87522750insT (hg38) ; chr7:g.87522748_87522749insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87522756dup , CM000669.2:g.87522756dup	GRCh38
NC_000007.13:g.87152072dup , CM000669.1:g.87152072dup	GRCh37
NC_000007.12:g.86990008dup	NCBI36
NG_011513.1:g.195500dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2686-1873dup	ENSP00000265724.3:n.2686-1873dup
ENST00000622132.5:c.2686-1873dup MANE Select	ENSP00000478255.1:n.2686-1873dup
ENST00000265724.7:c.2686-1873dup	ENSP00000265724.3:n.2686-1873dup
ENST00000488737.6:n.328-1873dup
ENST00000496821.5:n.314-1873dup
ENST00000543898.5:c.2494-1873dup	ENSP00000444095.1:n.2494-1873dup
ENST00000622132.4:c.2686-1873dup	ENSP00000478255.1:n.2686-1873dup
NM_000927.4:c.2686-1873dup	NP_000918.2:n.2686-1873dup
NM_001348944.1:c.2686-1873dup	NP_001335873.1:n.2686-1873dup
NM_001348945.1:c.2896-1873dup	NP_001335874.1:n.2896-1873dup
NM_001348946.1:c.2686-1873dup	NP_001335875.1:n.2686-1873dup
NM_001348946.2:c.2686-1873dup MANE Select	NP_001335875.1:n.2686-1873dup
NM_000927.5:c.2686-1873dup	NP_000918.2:n.2686-1873dup
NM_001348944.2:c.2686-1873dup	NP_001335873.1:n.2686-1873dup
NM_001348945.2:c.2896-1873dup	NP_001335874.1:n.2896-1873dup