Canonical Allele Identifier: CA456356262

Gene: ABCB1

Linked Data

• dbSNP Id: rs1241023862
• gnomAD v2: 7-87160146-C-CAAGA
• gnomAD v3: 7-87530830-C-CAAGA
• gnomAD v4: 7-87530830-C-CAAGA
• MyVariant Identifiers: chr7:g.87160154_87160166delinsAAAGCAAGAAAGAAAGA (hg19) ; chr7:g.87160146_87160147insAAGA (hg19) ; chr7:g.87530838_87530850delinsAAAGCAAGAAAGAAAGA (hg38) ; chr7:g.87530830_87530831insAAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530834_87530837dup , CM000669.2:g.87530834_87530837dup	GRCh38
NC_000007.13:g.87160150_87160153dup , CM000669.1:g.87160150_87160153dup	GRCh37
NC_000007.12:g.86998086_86998089dup	NCBI36
NG_011513.1:g.187415_187418dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+460_2685+463dup	ENSP00000265724.3:n.2685+460_2685+463dup
ENST00000622132.5:c.2685+460_2685+463dup MANE Select	ENSP00000478255.1:n.2685+460_2685+463dup
ENST00000265724.7:c.2685+460_2685+463dup	ENSP00000265724.3:n.2685+460_2685+463dup
ENST00000488737.6:n.327+460_327+463dup
ENST00000496821.5:n.313+460_313+463dup
ENST00000543898.5:c.2493+460_2493+463dup	ENSP00000444095.1:n.2493+460_2493+463dup
ENST00000622132.4:c.2685+460_2685+463dup	ENSP00000478255.1:n.2685+460_2685+463dup
NM_000927.4:c.2685+460_2685+463dup	NP_000918.2:n.2685+460_2685+463dup
NM_001348944.1:c.2685+460_2685+463dup	NP_001335873.1:n.2685+460_2685+463dup
NM_001348945.1:c.2895+460_2895+463dup	NP_001335874.1:n.2895+460_2895+463dup
NM_001348946.1:c.2685+460_2685+463dup	NP_001335875.1:n.2685+460_2685+463dup
NM_001348946.2:c.2685+460_2685+463dup MANE Select	NP_001335875.1:n.2685+460_2685+463dup
NM_000927.5:c.2685+460_2685+463dup	NP_000918.2:n.2685+460_2685+463dup
NM_001348944.2:c.2685+460_2685+463dup	NP_001335873.1:n.2685+460_2685+463dup
NM_001348945.2:c.2895+460_2895+463dup	NP_001335874.1:n.2895+460_2895+463dup