Canonical Allele Identifier: CA1723638413

Gene: ABCB1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87591570A>T , CM000669.2:g.87591570A>T	GRCh38
NC_000007.13:g.87220886A>T , CM000669.1:g.87220886A>T	GRCh37
NC_000007.12:g.87058822A>T	NCBI36
NG_011513.1:g.126679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.117+4196T>A	ENSP00000265724.3:n.117+4196T>A
ENST00000622132.5:c.117+4196T>A MANE Select	ENSP00000478255.1:n.117+4196T>A
ENST00000265724.7:c.117+4196T>A	ENSP00000265724.3:n.117+4196T>A
ENST00000416177.1:c.117+4196T>A	ENSP00000399419.1:n.117+4196T>A
ENST00000543898.5:c.117+4196T>A	ENSP00000444095.1:n.117+4196T>A
ENST00000622132.4:c.117+4196T>A	ENSP00000478255.1:n.117+4196T>A
NM_000927.4:c.117+4196T>A	NP_000918.2:n.117+4196T>A
NM_001348944.1:c.117+4196T>A	NP_001335873.1:n.117+4196T>A
NM_001348945.1:c.327+4196T>A	NP_001335874.1:n.327+4196T>A
NM_001348946.1:c.117+4196T>A	NP_001335875.1:n.117+4196T>A
NM_001348946.2:c.117+4196T>A MANE Select	NP_001335875.1:n.117+4196T>A
NM_000927.5:c.117+4196T>A	NP_000918.2:n.117+4196T>A
NM_001348944.2:c.117+4196T>A	NP_001335873.1:n.117+4196T>A
NM_001348945.2:c.327+4196T>A	NP_001335874.1:n.327+4196T>A