Canonical Allele Identifier: CA4327896

Gene: ABCB1

Linked Data

• dbSNP Id: rs781068922
• ExAC: 7:87145977 A / T
• gnomAD v2: 7-87145977-A-T
• gnomAD v4: 7-87516661-A-T
• MyVariant Identifiers: chr7:g.87145977A>T (hg19) ; chr7:g.87516661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516661A>T , CM000669.2:g.87516661A>T	GRCh38
NC_000007.13:g.87145977A>T , CM000669.1:g.87145977A>T	GRCh37
NC_000007.12:g.86983913A>T	NCBI36
NG_011513.1:g.201588T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2932T>A	ENSP00000265724.3:p.Phe978Ile
ENST00000622132.5:c.2932T>A MANE Select	ENSP00000478255.1:p.Phe978Ile
ENST00000265724.7:c.2932T>A	ENSP00000265724.3:p.Phe978Ile
ENST00000475929.5:n.88T>A
ENST00000483831.1:n.490T>A
ENST00000488737.6:n.574T>A
ENST00000496821.5:n.560T>A
ENST00000543898.5:c.2740T>A	ENSP00000444095.1:p.Phe914Ile
ENST00000622132.4:c.2932T>A	ENSP00000478255.1:p.Phe978Ile
NM_000927.4:c.2932T>A	NP_000918.2:p.Phe978Ile
NM_001348944.1:c.2932T>A	NP_001335873.1:p.Phe978Ile
NM_001348945.1:c.3142T>A	NP_001335874.1:p.Phe1048Ile
NM_001348946.1:c.2932T>A	NP_001335875.1:p.Phe978Ile
NM_001348946.2:c.2932T>A MANE Select	NP_001335875.1:p.Phe978Ile
NM_000927.5:c.2932T>A	NP_000918.2:p.Phe978Ile
NM_001348944.2:c.2932T>A	NP_001335873.1:p.Phe978Ile
NM_001348945.2:c.3142T>A	NP_001335874.1:p.Phe1048Ile