Canonical Allele Identifier: CA456349757

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87516575-G-A
• MyVariant Identifiers: chr7:g.87145891G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516575G>A , CM000669.2:g.87516575G>A	GRCh38
NC_000007.13:g.87145891G>A , CM000669.1:g.87145891G>A	GRCh37
NC_000007.12:g.86983827G>A	NCBI36
NG_011513.1:g.201674C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3018C>T	ENSP00000265724.3:p.Ala1006=
ENST00000622132.5:c.3018C>T MANE Select	ENSP00000478255.1:p.Ala1006=
ENST00000265724.7:c.3018C>T	ENSP00000265724.3:p.Ala1006=
ENST00000475929.5:n.174C>T
ENST00000483831.1:n.576C>T
ENST00000488737.6:n.660C>T
ENST00000496821.5:n.646C>T
ENST00000543898.5:c.2826C>T	ENSP00000444095.1:p.Ala942=
ENST00000622132.4:c.3018C>T	ENSP00000478255.1:p.Ala1006=
NM_000927.4:c.3018C>T	NP_000918.2:p.Ala1006=
NM_001348944.1:c.3018C>T	NP_001335873.1:p.Ala1006=
NM_001348945.1:c.3228C>T	NP_001335874.1:p.Ala1076=
NM_001348946.1:c.3018C>T	NP_001335875.1:p.Ala1006=
NM_001348946.2:c.3018C>T MANE Select	NP_001335875.1:p.Ala1006=
NM_000927.5:c.3018C>T	NP_000918.2:p.Ala1006=
NM_001348944.2:c.3018C>T	NP_001335873.1:p.Ala1006=
NM_001348945.2:c.3228C>T	NP_001335874.1:p.Ala1076=