Canonical Allele Identifier: CA843416664

Gene: ABCB1

Linked Data

• dbSNP Id: rs1164810899
• MyVariant Identifiers: chr7:g.87144432A>C (hg19) ; chr7:g.87515116A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515116A>C , CM000669.2:g.87515116A>C	GRCh38
NC_000007.13:g.87144432A>C , CM000669.1:g.87144432A>C	GRCh37
NC_000007.12:g.86982368A>C	NCBI36
NG_011513.1:g.203133T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3282+115T>G	ENSP00000265724.3:n.3282+115T>G
ENST00000622132.5:c.3282+115T>G MANE Select	ENSP00000478255.1:n.3282+115T>G
ENST00000265724.7:c.3282+115T>G	ENSP00000265724.3:n.3282+115T>G
ENST00000475929.5:n.438+115T>G
ENST00000488737.6:n.924+115T>G
ENST00000543898.5:c.3090+115T>G	ENSP00000444095.1:n.3090+115T>G
ENST00000622132.4:c.3282+115T>G	ENSP00000478255.1:n.3282+115T>G
NM_000927.4:c.3282+115T>G	NP_000918.2:n.3282+115T>G
NM_001348944.1:c.3282+115T>G	NP_001335873.1:n.3282+115T>G
NM_001348945.1:c.3492+115T>G	NP_001335874.1:n.3492+115T>G
NM_001348946.1:c.3282+115T>G	NP_001335875.1:n.3282+115T>G
NM_001348946.2:c.3282+115T>G MANE Select	NP_001335875.1:n.3282+115T>G
NM_000927.5:c.3282+115T>G	NP_000918.2:n.3282+115T>G
NM_001348944.2:c.3282+115T>G	NP_001335873.1:n.3282+115T>G
NM_001348945.2:c.3492+115T>G	NP_001335874.1:n.3492+115T>G