Canonical Allele Identifier: CA368044802

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87144723T>G (hg19) ; chr7:g.87515407T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515407T>G , CM000669.2:g.87515407T>G	GRCh38
NC_000007.13:g.87144723T>G , CM000669.1:g.87144723T>G	GRCh37
NC_000007.12:g.86982659T>G	NCBI36
NG_011513.1:g.202842A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3106A>C	ENSP00000265724.3:p.Thr1036Pro
ENST00000622132.5:c.3106A>C MANE Select	ENSP00000478255.1:p.Thr1036Pro
ENST00000265724.7:c.3106A>C	ENSP00000265724.3:p.Thr1036Pro
ENST00000475929.5:n.262A>C
ENST00000488737.6:n.748A>C
ENST00000496821.5:n.734A>C
ENST00000543898.5:c.2914A>C	ENSP00000444095.1:p.Thr972Pro
ENST00000622132.4:c.3106A>C	ENSP00000478255.1:p.Thr1036Pro
NM_000927.4:c.3106A>C	NP_000918.2:p.Thr1036Pro
NM_001348944.1:c.3106A>C	NP_001335873.1:p.Thr1036Pro
NM_001348945.1:c.3316A>C	NP_001335874.1:p.Thr1106Pro
NM_001348946.1:c.3106A>C	NP_001335875.1:p.Thr1036Pro
NM_001348946.2:c.3106A>C MANE Select	NP_001335875.1:p.Thr1036Pro
NM_000927.5:c.3106A>C	NP_000918.2:p.Thr1036Pro
NM_001348944.2:c.3106A>C	NP_001335873.1:p.Thr1036Pro
NM_001348945.2:c.3316A>C	NP_001335874.1:p.Thr1106Pro