Canonical Allele Identifier: CA2578930185

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550398T>C , CM000669.2:g.87550398T>C	GRCh38
NC_000007.13:g.87179714T>C , CM000669.1:g.87179714T>C	GRCh37
NC_000007.12:g.87017650T>C	NCBI36
NG_011513.1:g.167851A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1224+70A>G	ENSP00000265724.3:n.1224+70A>G
ENST00000622132.5:c.1224+70A>G MANE Select	ENSP00000478255.1:n.1224+70A>G
ENST00000265724.7:c.1224+70A>G	ENSP00000265724.3:n.1224+70A>G
ENST00000543898.5:c.1032+70A>G	ENSP00000444095.1:n.1032+70A>G
ENST00000622132.4:c.1224+70A>G	ENSP00000478255.1:n.1224+70A>G
NM_000927.4:c.1224+70A>G	NP_000918.2:n.1224+70A>G
NM_001348944.1:c.1224+70A>G	NP_001335873.1:n.1224+70A>G
NM_001348945.1:c.1434+70A>G	NP_001335874.1:n.1434+70A>G
NM_001348946.1:c.1224+70A>G	NP_001335875.1:n.1224+70A>G
NM_001348946.2:c.1224+70A>G MANE Select	NP_001335875.1:n.1224+70A>G
NM_000927.5:c.1224+70A>G	NP_000918.2:n.1224+70A>G
NM_001348944.2:c.1224+70A>G	NP_001335873.1:n.1224+70A>G
NM_001348945.2:c.1434+70A>G	NP_001335874.1:n.1434+70A>G