Canonical Allele Identifier: CA843389071

Gene: ABCB1

Linked Data

• dbSNP Id: rs1375390997
• gnomAD v3: 7-87550387-C-CT
• gnomAD v4: 7-87550387-C-CT
• MyVariant Identifiers: chr7:g.87179703_87179704insT (hg19) ; chr7:g.87550387_87550388insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550393dup , CM000669.2:g.87550393dup	GRCh38
NC_000007.13:g.87179709dup , CM000669.1:g.87179709dup	GRCh37
NC_000007.12:g.87017645dup	NCBI36
NG_011513.1:g.167861dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1224+80dup	ENSP00000265724.3:n.1224+80dup
ENST00000622132.5:c.1224+80dup MANE Select	ENSP00000478255.1:n.1224+80dup
ENST00000265724.7:c.1224+80dup	ENSP00000265724.3:n.1224+80dup
ENST00000543898.5:c.1032+80dup	ENSP00000444095.1:n.1032+80dup
ENST00000622132.4:c.1224+80dup	ENSP00000478255.1:n.1224+80dup
NM_000927.4:c.1224+80dup	NP_000918.2:n.1224+80dup
NM_001348944.1:c.1224+80dup	NP_001335873.1:n.1224+80dup
NM_001348945.1:c.1434+80dup	NP_001335874.1:n.1434+80dup
NM_001348946.1:c.1224+80dup	NP_001335875.1:n.1224+80dup
NM_001348946.2:c.1224+80dup MANE Select	NP_001335875.1:n.1224+80dup
NM_000927.5:c.1224+80dup	NP_000918.2:n.1224+80dup
NM_001348944.2:c.1224+80dup	NP_001335873.1:n.1224+80dup
NM_001348945.2:c.1434+80dup	NP_001335874.1:n.1434+80dup