Canonical Allele Identifier: CA2683605974

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87531717-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531717A>C , CM000669.2:g.87531717A>C	GRCh38
NC_000007.13:g.87161033A>C , CM000669.1:g.87161033A>C	GRCh37
NC_000007.12:g.86998969A>C	NCBI36
NG_011513.1:g.186532T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2482-220T>G	ENSP00000265724.3:n.2482-220T>G
ENST00000622132.5:c.2482-220T>G MANE Select	ENSP00000478255.1:n.2482-220T>G
ENST00000265724.7:c.2482-220T>G	ENSP00000265724.3:n.2482-220T>G
ENST00000496821.5:n.110-220T>G
ENST00000543898.5:c.2290-220T>G	ENSP00000444095.1:n.2290-220T>G
ENST00000622132.4:c.2482-220T>G	ENSP00000478255.1:n.2482-220T>G
NM_000927.4:c.2482-220T>G	NP_000918.2:n.2482-220T>G
NM_001348944.1:c.2482-220T>G	NP_001335873.1:n.2482-220T>G
NM_001348945.1:c.2692-220T>G	NP_001335874.1:n.2692-220T>G
NM_001348946.1:c.2482-220T>G	NP_001335875.1:n.2482-220T>G
NM_001348946.2:c.2482-220T>G MANE Select	NP_001335875.1:n.2482-220T>G
NM_000927.5:c.2482-220T>G	NP_000918.2:n.2482-220T>G
NM_001348944.2:c.2482-220T>G	NP_001335873.1:n.2482-220T>G
NM_001348945.2:c.2692-220T>G	NP_001335874.1:n.2692-220T>G