Canonical Allele Identifier: CA843416672

Gene: ABCB1

Linked Data

• dbSNP Id: rs1426233863
• MyVariant Identifiers: chr7:g.87144437G>A (hg19) ; chr7:g.87515121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515121G>A , CM000669.2:g.87515121G>A	GRCh38
NC_000007.13:g.87144437G>A , CM000669.1:g.87144437G>A	GRCh37
NC_000007.12:g.86982373G>A	NCBI36
NG_011513.1:g.203128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3282+110C>T	ENSP00000265724.3:n.3282+110C>T
ENST00000622132.5:c.3282+110C>T MANE Select	ENSP00000478255.1:n.3282+110C>T
ENST00000265724.7:c.3282+110C>T	ENSP00000265724.3:n.3282+110C>T
ENST00000475929.5:n.438+110C>T
ENST00000488737.6:n.924+110C>T
ENST00000543898.5:c.3090+110C>T	ENSP00000444095.1:n.3090+110C>T
ENST00000622132.4:c.3282+110C>T	ENSP00000478255.1:n.3282+110C>T
NM_000927.4:c.3282+110C>T	NP_000918.2:n.3282+110C>T
NM_001348944.1:c.3282+110C>T	NP_001335873.1:n.3282+110C>T
NM_001348945.1:c.3492+110C>T	NP_001335874.1:n.3492+110C>T
NM_001348946.1:c.3282+110C>T	NP_001335875.1:n.3282+110C>T
NM_001348946.2:c.3282+110C>T MANE Select	NP_001335875.1:n.3282+110C>T
NM_000927.5:c.3282+110C>T	NP_000918.2:n.3282+110C>T
NM_001348944.2:c.3282+110C>T	NP_001335873.1:n.3282+110C>T
NM_001348945.2:c.3492+110C>T	NP_001335874.1:n.3492+110C>T