Canonical Allele Identifier: CA1723658881
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87585461C= , CM000669.2:g.87585461C= GRCh38
NC_000007.13:g.87214777C= , CM000669.1:g.87214777C= GRCh37
NC_000007.12:g.87052713C= NCBI36
NG_011513.1:g.132788G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.286+51G= ENSP00000265724.3:n.286+51G=
ENST00000622132.5:c.286+51G= MANE Select ENSP00000478255.1:n.286+51G=
ENST00000265724.7:c.286+51G= ENSP00000265724.3:n.286+51G=
ENST00000543898.5:c.286+51G= ENSP00000444095.1:n.286+51G=
ENST00000622132.4:c.286+51G= ENSP00000478255.1:n.286+51G=
NM_000927.4:c.286+51G= NP_000918.2:n.286+51G=
NM_001348944.1:c.286+51G= NP_001335873.1:n.286+51G=
NM_001348945.1:c.496+51G= NP_001335874.1:n.496+51G=
NM_001348946.1:c.286+51G= NP_001335875.1:n.286+51G=
NM_001348946.2:c.286+51G= MANE Select NP_001335875.1:n.286+51G=
NM_000927.5:c.286+51G= NP_000918.2:n.286+51G=
NM_001348944.2:c.286+51G= NP_001335873.1:n.286+51G=
NM_001348945.2:c.496+51G= NP_001335874.1:n.496+51G=