Canonical Allele Identifier: CA368055713

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87165778T>A (hg19) ; chr7:g.87536462T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87536462T>A , CM000669.2:g.87536462T>A	GRCh38
NC_000007.13:g.87165778T>A , CM000669.1:g.87165778T>A	GRCh37
NC_000007.12:g.87003714T>A	NCBI36
NG_011513.1:g.181787A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2477A>T	ENSP00000265724.3:p.Lys826Ile
ENST00000622132.5:c.2477A>T MANE Select	ENSP00000478255.1:p.Lys826Ile
ENST00000265724.7:c.2477A>T	ENSP00000265724.3:p.Lys826Ile
ENST00000496821.5:n.105A>T
ENST00000543898.5:c.2285A>T	ENSP00000444095.1:p.Lys762Ile
ENST00000622132.4:c.2477A>T	ENSP00000478255.1:p.Lys826Ile
NM_000927.4:c.2477A>T	NP_000918.2:p.Lys826Ile
NM_001348944.1:c.2477A>T	NP_001335873.1:p.Lys826Ile
NM_001348945.1:c.2687A>T	NP_001335874.1:p.Lys896Ile
NM_001348946.1:c.2477A>T	NP_001335875.1:p.Lys826Ile
NM_001348946.2:c.2477A>T MANE Select	NP_001335875.1:p.Lys826Ile
NM_000927.5:c.2477A>T	NP_000918.2:p.Lys826Ile
NM_001348944.2:c.2477A>T	NP_001335873.1:p.Lys826Ile
NM_001348945.2:c.2687A>T	NP_001335874.1:p.Lys896Ile