Canonical Allele Identifier: CA456349703

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87145831T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516515T>A , CM000669.2:g.87516515T>A	GRCh38
NC_000007.13:g.87145831T>A , CM000669.1:g.87145831T>A	GRCh37
NC_000007.12:g.86983767T>A	NCBI36
NG_011513.1:g.201734A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.3078A>T	ENSP00000265724.3:p.Leu1026=
ENST00000622132.5:c.3078A>T MANE Select	ENSP00000478255.1:p.Leu1026=
ENST00000265724.7:c.3078A>T	ENSP00000265724.3:p.Leu1026=
ENST00000475929.5:n.234A>T
ENST00000483831.1:n.636A>T
ENST00000488737.6:n.720A>T
ENST00000496821.5:n.706A>T
ENST00000543898.5:c.2886A>T	ENSP00000444095.1:p.Leu962=
ENST00000622132.4:c.3078A>T	ENSP00000478255.1:p.Leu1026=
NM_000927.4:c.3078A>T	NP_000918.2:p.Leu1026=
NM_001348944.1:c.3078A>T	NP_001335873.1:p.Leu1026=
NM_001348945.1:c.3288A>T	NP_001335874.1:p.Leu1096=
NM_001348946.1:c.3078A>T	NP_001335875.1:p.Leu1026=
NM_001348946.2:c.3078A>T MANE Select	NP_001335875.1:p.Leu1026=
NM_000927.5:c.3078A>T	NP_000918.2:p.Leu1026=
NM_001348944.2:c.3078A>T	NP_001335873.1:p.Leu1026=
NM_001348945.2:c.3288A>T	NP_001335874.1:p.Leu1096=