Canonical Allele Identifier: CA1723658199
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87583947T= , CM000669.2:g.87583947T= GRCh38
NC_000007.13:g.87213263T= , CM000669.1:g.87213263T= GRCh37
NC_000007.12:g.87051199T= NCBI36
NG_011513.1:g.134302A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.286+1565A= ENSP00000265724.3:n.286+1565A=
ENST00000622132.5:c.286+1565A= MANE Select ENSP00000478255.1:n.286+1565A=
ENST00000265724.7:c.286+1565A= ENSP00000265724.3:n.286+1565A=
ENST00000543898.5:c.286+1565A= ENSP00000444095.1:n.286+1565A=
ENST00000622132.4:c.286+1565A= ENSP00000478255.1:n.286+1565A=
NM_000927.4:c.286+1565A= NP_000918.2:n.286+1565A=
NM_001348944.1:c.286+1565A= NP_001335873.1:n.286+1565A=
NM_001348945.1:c.496+1565A= NP_001335874.1:n.496+1565A=
NM_001348946.1:c.286+1565A= NP_001335875.1:n.286+1565A=
NM_001348946.2:c.286+1565A= MANE Select NP_001335875.1:n.286+1565A=
NM_000927.5:c.286+1565A= NP_000918.2:n.286+1565A=
NM_001348944.2:c.286+1565A= NP_001335873.1:n.286+1565A=
NM_001348945.2:c.496+1565A= NP_001335874.1:n.496+1565A=