Canonical Allele Identifier: CA162474291

Gene: ABCB1

Linked Data

• dbSNP Id: rs34976462
• MyVariant Identifiers: chr7:g.87230209G>T (hg19) ; chr7:g.87600893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600893G>T , CM000669.2:g.87600893G>T	GRCh38
NC_000007.13:g.87230209G>T , CM000669.1:g.87230209G>T	GRCh37
NC_000007.12:g.87068145G>T	NCBI36
NG_011513.1:g.117356C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-145C>A	ENSP00000265724.3:n.-145C>A
ENST00000265724.7:c.-145C>A	ENSP00000265724.3:n.-145C>A
ENST00000416177.1:c.-77-68C>A	ENSP00000399419.1:n.-77-68C>A
ENST00000476862.1:n.502C>A
ENST00000543898.5:c.-145C>A	ENSP00000444095.1:n.-145C>A
ENST00000622132.4:c.-145C>A	ENSP00000478255.1:n.-145C>A
NM_000927.4:c.-145C>A	NP_000918.2:n.-145C>A
NM_001348944.1:c.-77-68C>A	NP_001335873.1:n.-77-68C>A
NM_001348945.1:c.134-68C>A	NP_001335874.1:n.134-68C>A
NM_000927.5:c.-145C>A	NP_000918.2:n.-145C>A
NM_001348944.2:c.-77-68C>A	NP_001335873.1:n.-77-68C>A
NM_001348945.2:c.134-68C>A	NP_001335874.1:n.134-68C>A