Canonical Allele Identifier: CA1723646871

Gene: ABCB1

Linked Data

• dbSNP Id: rs28381919

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87545162_87545171dup , CM000669.2:g.87545162_87545171dup	GRCh38
NC_000007.13:g.87174478_87174487dup , CM000669.1:g.87174478_87174487dup	GRCh37
NC_000007.12:g.87012414_87012423dup	NCBI36
NG_011513.1:g.173095_173104dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1888-155_1888-146dup	ENSP00000265724.3:n.1888-155_1888-146dup
ENST00000622132.5:c.1888-155_1888-146dup MANE Select	ENSP00000478255.1:n.1888-155_1888-146dup
ENST00000265724.7:c.1888-155_1888-146dup	ENSP00000265724.3:n.1888-155_1888-146dup
ENST00000543898.5:c.1696-155_1696-146dup	ENSP00000444095.1:n.1696-155_1696-146dup
ENST00000622132.4:c.1888-155_1888-146dup	ENSP00000478255.1:n.1888-155_1888-146dup
NM_000927.4:c.1888-155_1888-146dup	NP_000918.2:n.1888-155_1888-146dup
NM_001348944.1:c.1888-155_1888-146dup	NP_001335873.1:n.1888-155_1888-146dup
NM_001348945.1:c.2098-155_2098-146dup	NP_001335874.1:n.2098-155_2098-146dup
NM_001348946.1:c.1888-155_1888-146dup	NP_001335875.1:n.1888-155_1888-146dup
NM_001348946.2:c.1888-155_1888-146dup MANE Select	NP_001335875.1:n.1888-155_1888-146dup
NM_000927.5:c.1888-155_1888-146dup	NP_000918.2:n.1888-155_1888-146dup
NM_001348944.2:c.1888-155_1888-146dup	NP_001335873.1:n.1888-155_1888-146dup
NM_001348945.2:c.2098-155_2098-146dup	NP_001335874.1:n.2098-155_2098-146dup