Canonical Allele Identifier: CA1723658506
Gene: ABCB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87584660A= , CM000669.2:g.87584660A= GRCh38
NC_000007.13:g.87213976A= , CM000669.1:g.87213976A= GRCh37
NC_000007.12:g.87051912A= NCBI36
NG_011513.1:g.133589T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.286+852T= ENSP00000265724.3:n.286+852T=
ENST00000622132.5:c.286+852T= MANE Select ENSP00000478255.1:n.286+852T=
ENST00000265724.7:c.286+852T= ENSP00000265724.3:n.286+852T=
ENST00000543898.5:c.286+852T= ENSP00000444095.1:n.286+852T=
ENST00000622132.4:c.286+852T= ENSP00000478255.1:n.286+852T=
NM_000927.4:c.286+852T= NP_000918.2:n.286+852T=
NM_001348944.1:c.286+852T= NP_001335873.1:n.286+852T=
NM_001348945.1:c.496+852T= NP_001335874.1:n.496+852T=
NM_001348946.1:c.286+852T= NP_001335875.1:n.286+852T=
NM_001348946.2:c.286+852T= MANE Select NP_001335875.1:n.286+852T=
NM_000927.5:c.286+852T= NP_000918.2:n.286+852T=
NM_001348944.2:c.286+852T= NP_001335873.1:n.286+852T=
NM_001348945.2:c.496+852T= NP_001335874.1:n.496+852T=
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