Canonical Allele Identifier: CA456449960

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87179305C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87549989C>T , CM000669.2:g.87549989C>T	GRCh38
NC_000007.13:g.87179305C>T , CM000669.1:g.87179305C>T	GRCh37
NC_000007.12:g.87017241C>T	NCBI36
NG_011513.1:g.168260G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1416G>A	ENSP00000265724.3:p.Val472=
ENST00000622132.5:c.1416G>A MANE Select	ENSP00000478255.1:p.Val472=
ENST00000265724.7:c.1416G>A	ENSP00000265724.3:p.Val472=
ENST00000482527.1:n.170G>A
ENST00000543898.5:c.1224G>A	ENSP00000444095.1:p.Val408=
ENST00000622132.4:c.1416G>A	ENSP00000478255.1:p.Val472=
NM_000927.4:c.1416G>A	NP_000918.2:p.Val472=
NM_001348944.1:c.1416G>A	NP_001335873.1:p.Val472=
NM_001348945.1:c.1626G>A	NP_001335874.1:p.Val542=
NM_001348946.1:c.1416G>A	NP_001335875.1:p.Val472=
NM_001348946.2:c.1416G>A MANE Select	NP_001335875.1:p.Val472=
NM_000927.5:c.1416G>A	NP_000918.2:p.Val472=
NM_001348944.2:c.1416G>A	NP_001335873.1:p.Val472=
NM_001348945.2:c.1626G>A	NP_001335874.1:p.Val542=