Canonical Allele Identifier: CA162474293

Gene: ABCB1

Linked Data

• dbSNP Id: rs952525996
• MyVariant Identifiers: chr7:g.87230217T>C (hg19) ; chr7:g.87600901T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600901T>C , CM000669.2:g.87600901T>C	GRCh38
NC_000007.13:g.87230217T>C , CM000669.1:g.87230217T>C	GRCh37
NC_000007.12:g.87068153T>C	NCBI36
NG_011513.1:g.117348A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-153A>G	ENSP00000265724.3:n.-153A>G
ENST00000265724.7:c.-153A>G	ENSP00000265724.3:n.-153A>G
ENST00000416177.1:c.-78+72A>G	ENSP00000399419.1:n.-78+72A>G
ENST00000476862.1:n.494A>G
ENST00000543898.5:c.-153A>G	ENSP00000444095.1:n.-153A>G
ENST00000622132.4:c.-153A>G	ENSP00000478255.1:n.-153A>G
NM_000927.4:c.-153A>G	NP_000918.2:n.-153A>G
NM_001348944.1:c.-78+72A>G	NP_001335873.1:n.-78+72A>G
NM_001348945.1:c.133+72A>G	NP_001335874.1:n.133+72A>G
NM_000927.5:c.-153A>G	NP_000918.2:n.-153A>G
NM_001348944.2:c.-78+72A>G	NP_001335873.1:n.-78+72A>G
NM_001348945.2:c.133+72A>G	NP_001335874.1:n.133+72A>G