Canonical Allele Identifier: CA2715247242

Gene: ABCB1

Linked Data

• dbSNP Id: rs2117129538

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531274T>A , CM000669.2:g.87531274T>A	GRCh38
NC_000007.13:g.87160590T>A , CM000669.1:g.87160590T>A	GRCh37
NC_000007.12:g.86998526T>A	NCBI36
NG_011513.1:g.186975A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2685+20A>T	ENSP00000265724.3:n.2685+20A>T
ENST00000622132.5:c.2685+20A>T MANE Select	ENSP00000478255.1:n.2685+20A>T
ENST00000265724.7:c.2685+20A>T	ENSP00000265724.3:n.2685+20A>T
ENST00000488737.6:n.327+20A>T
ENST00000496821.5:n.313+20A>T
ENST00000543898.5:c.2493+20A>T	ENSP00000444095.1:n.2493+20A>T
ENST00000622132.4:c.2685+20A>T	ENSP00000478255.1:n.2685+20A>T
NM_000927.4:c.2685+20A>T	NP_000918.2:n.2685+20A>T
NM_001348944.1:c.2685+20A>T	NP_001335873.1:n.2685+20A>T
NM_001348945.1:c.2895+20A>T	NP_001335874.1:n.2895+20A>T
NM_001348946.1:c.2685+20A>T	NP_001335875.1:n.2685+20A>T
NM_001348946.2:c.2685+20A>T MANE Select	NP_001335875.1:n.2685+20A>T
NM_000927.5:c.2685+20A>T	NP_000918.2:n.2685+20A>T
NM_001348944.2:c.2685+20A>T	NP_001335873.1:n.2685+20A>T
NM_001348945.2:c.2895+20A>T	NP_001335874.1:n.2895+20A>T