Canonical Allele Identifier: CA456359347

Gene: ABCB1

Linked Data

• dbSNP Id: rs143696486
• MyVariant Identifiers: chr7:g.87179571C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550255C>A , CM000669.2:g.87550255C>A	GRCh38
NC_000007.13:g.87179571C>A , CM000669.1:g.87179571C>A	GRCh37
NC_000007.12:g.87017507C>A	NCBI36
NG_011513.1:g.167994G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1266G>T	ENSP00000265724.3:p.Thr422=
ENST00000622132.5:c.1266G>T MANE Select	ENSP00000478255.1:p.Thr422=
ENST00000265724.7:c.1266G>T	ENSP00000265724.3:p.Thr422=
ENST00000543898.5:c.1074G>T	ENSP00000444095.1:p.Thr358=
ENST00000622132.4:c.1266G>T	ENSP00000478255.1:p.Thr422=
NM_000927.4:c.1266G>T	NP_000918.2:p.Thr422=
NM_001348944.1:c.1266G>T	NP_001335873.1:p.Thr422=
NM_001348945.1:c.1476G>T	NP_001335874.1:p.Thr492=
NM_001348946.1:c.1266G>T	NP_001335875.1:p.Thr422=
NM_001348946.2:c.1266G>T MANE Select	NP_001335875.1:p.Thr422=
NM_000927.5:c.1266G>T	NP_000918.2:p.Thr422=
NM_001348944.2:c.1266G>T	NP_001335873.1:p.Thr422=
NM_001348945.2:c.1476G>T	NP_001335874.1:p.Thr492=