Canonical Allele Identifier: CA368062348

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816977747
• gnomAD v3: 7-87549999-A-G
• gnomAD v4: 7-87549999-A-G
• MyVariant Identifiers: chr7:g.87179315A>G (hg19) ; chr7:g.87549999A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87549999A>G , CM000669.2:g.87549999A>G	GRCh38
NC_000007.13:g.87179315A>G , CM000669.1:g.87179315A>G	GRCh37
NC_000007.12:g.87017251A>G	NCBI36
NG_011513.1:g.168250T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1406T>C	ENSP00000265724.3:p.Ile469Thr
ENST00000622132.5:c.1406T>C MANE Select	ENSP00000478255.1:p.Ile469Thr
ENST00000265724.7:c.1406T>C	ENSP00000265724.3:p.Ile469Thr
ENST00000482527.1:n.160T>C
ENST00000543898.5:c.1214T>C	ENSP00000444095.1:p.Ile405Thr
ENST00000622132.4:c.1406T>C	ENSP00000478255.1:p.Ile469Thr
NM_000927.4:c.1406T>C	NP_000918.2:p.Ile469Thr
NM_001348944.1:c.1406T>C	NP_001335873.1:p.Ile469Thr
NM_001348945.1:c.1616T>C	NP_001335874.1:p.Ile539Thr
NM_001348946.1:c.1406T>C	NP_001335875.1:p.Ile469Thr
NM_001348946.2:c.1406T>C MANE Select	NP_001335875.1:p.Ile469Thr
NM_000927.5:c.1406T>C	NP_000918.2:p.Ile469Thr
NM_001348944.2:c.1406T>C	NP_001335873.1:p.Ile469Thr
NM_001348945.2:c.1616T>C	NP_001335874.1:p.Ile539Thr