Canonical Allele Identifier: CA2683604468

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87503877-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503877A>C , CM000669.2:g.87503877A>C	GRCh38
NC_000007.13:g.87133193A>C , CM000669.1:g.87133193A>C	GRCh37
NC_000007.12:g.86971129A>C	NCBI36
NG_011513.1:g.214372T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.*366T>G	ENSP00000265724.3:n.*366T>G
ENST00000622132.5:c.*366T>G MANE Select	ENSP00000478255.1:n.*366T>G
ENST00000265724.7:c.*366T>G	ENSP00000265724.3:n.*366T>G
ENST00000488737.6:n.1851T>G
ENST00000543898.5:c.*366T>G	ENSP00000444095.1:n.*366T>G
ENST00000622132.4:c.*366T>G	ENSP00000478255.1:n.*366T>G
NM_000927.4:c.*366T>G	NP_000918.2:n.*366T>G
NM_001348944.1:c.*366T>G	NP_001335873.1:n.*366T>G
NM_001348945.1:c.*366T>G	NP_001335874.1:n.*366T>G
NM_001348946.1:c.*366T>G	NP_001335875.1:n.*366T>G
NM_001348946.2:c.*366T>G MANE Select	NP_001335875.1:n.*366T>G
NM_000927.5:c.*366T>G	NP_000918.2:n.*366T>G
NM_001348944.2:c.*366T>G	NP_001335873.1:n.*366T>G
NM_001348945.2:c.*366T>G	NP_001335874.1:n.*366T>G