Canonical Allele Identifier: CA162123055

Gene: ABCB1

Linked Data

• dbSNP Id: rs41311775
• gnomAD v2: 7-87179511-C-T
• gnomAD v4: 7-87550195-C-T
• MyVariant Identifiers: chr7:g.87179511C>T (hg19) ; chr7:g.87550195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550195C>T , CM000669.2:g.87550195C>T	GRCh38
NC_000007.13:g.87179511C>T , CM000669.1:g.87179511C>T	GRCh37
NC_000007.12:g.87017447C>T	NCBI36
NG_011513.1:g.168054G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1326G>A	ENSP00000265724.3:p.Arg442=
ENST00000622132.5:c.1326G>A MANE Select	ENSP00000478255.1:p.Arg442=
ENST00000265724.7:c.1326G>A	ENSP00000265724.3:p.Arg442=
ENST00000543898.5:c.1134G>A	ENSP00000444095.1:p.Arg378=
ENST00000622132.4:c.1326G>A	ENSP00000478255.1:p.Arg442=
NM_000927.4:c.1326G>A	NP_000918.2:p.Arg442=
NM_001348944.1:c.1326G>A	NP_001335873.1:p.Arg442=
NM_001348945.1:c.1536G>A	NP_001335874.1:p.Arg512=
NM_001348946.1:c.1326G>A	NP_001335875.1:p.Arg442=
NM_001348946.2:c.1326G>A MANE Select	NP_001335875.1:p.Arg442=
NM_000927.5:c.1326G>A	NP_000918.2:p.Arg442=
NM_001348944.2:c.1326G>A	NP_001335873.1:p.Arg442=
NM_001348945.2:c.1536G>A	NP_001335874.1:p.Arg512=