Canonical Allele Identifier: CA162110735

Gene: ABCB1

Linked Data

• dbSNP Id: rs931003486
• gnomAD v3: 7-87531192-A-C
• gnomAD v4: 7-87531192-A-C
• MyVariant Identifiers: chr7:g.87160508A>C (hg19) ; chr7:g.87531192A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531192A>C , CM000669.2:g.87531192A>C	GRCh38
NC_000007.13:g.87160508A>C , CM000669.1:g.87160508A>C	GRCh37
NC_000007.12:g.86998444A>C	NCBI36
NG_011513.1:g.187057T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2685+102T>G	ENSP00000265724.3:n.2685+102T>G
ENST00000622132.5:c.2685+102T>G MANE Select	ENSP00000478255.1:n.2685+102T>G
ENST00000265724.7:c.2685+102T>G	ENSP00000265724.3:n.2685+102T>G
ENST00000488737.6:n.327+102T>G
ENST00000496821.5:n.313+102T>G
ENST00000543898.5:c.2493+102T>G	ENSP00000444095.1:n.2493+102T>G
ENST00000622132.4:c.2685+102T>G	ENSP00000478255.1:n.2685+102T>G
NM_000927.4:c.2685+102T>G	NP_000918.2:n.2685+102T>G
NM_001348944.1:c.2685+102T>G	NP_001335873.1:n.2685+102T>G
NM_001348945.1:c.2895+102T>G	NP_001335874.1:n.2895+102T>G
NM_001348946.1:c.2685+102T>G	NP_001335875.1:n.2685+102T>G
NM_001348946.2:c.2685+102T>G MANE Select	NP_001335875.1:n.2685+102T>G
NM_000927.5:c.2685+102T>G	NP_000918.2:n.2685+102T>G
NM_001348944.2:c.2685+102T>G	NP_001335873.1:n.2685+102T>G
NM_001348945.2:c.2895+102T>G	NP_001335874.1:n.2895+102T>G