Canonical Allele Identifier: CA2683607422

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87545109-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87545109C>A , CM000669.2:g.87545109C>A	GRCh38
NC_000007.13:g.87174425C>A , CM000669.1:g.87174425C>A	GRCh37
NC_000007.12:g.87012361C>A	NCBI36
NG_011513.1:g.173140G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.1888-110G>T	ENSP00000265724.3:n.1888-110G>T
ENST00000622132.5:c.1888-110G>T MANE Select	ENSP00000478255.1:n.1888-110G>T
ENST00000265724.7:c.1888-110G>T	ENSP00000265724.3:n.1888-110G>T
ENST00000543898.5:c.1696-110G>T	ENSP00000444095.1:n.1696-110G>T
ENST00000622132.4:c.1888-110G>T	ENSP00000478255.1:n.1888-110G>T
NM_000927.4:c.1888-110G>T	NP_000918.2:n.1888-110G>T
NM_001348944.1:c.1888-110G>T	NP_001335873.1:n.1888-110G>T
NM_001348945.1:c.2098-110G>T	NP_001335874.1:n.2098-110G>T
NM_001348946.1:c.1888-110G>T	NP_001335875.1:n.1888-110G>T
NM_001348946.2:c.1888-110G>T MANE Select	NP_001335875.1:n.1888-110G>T
NM_000927.5:c.1888-110G>T	NP_000918.2:n.1888-110G>T
NM_001348944.2:c.1888-110G>T	NP_001335873.1:n.1888-110G>T
NM_001348945.2:c.2098-110G>T	NP_001335874.1:n.2098-110G>T