Canonical Allele Identifier: CA1723651744
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87550379T= , CM000669.2:g.87550379T= GRCh38
NC_000007.13:g.87179695T= , CM000669.1:g.87179695T= GRCh37
NC_000007.12:g.87017631T= NCBI36
NG_011513.1:g.167870A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1225-83A= ENSP00000265724.3:n.1225-83A=
ENST00000622132.5:c.1225-83A= MANE Select ENSP00000478255.1:n.1225-83A=
ENST00000265724.7:c.1225-83A= ENSP00000265724.3:n.1225-83A=
ENST00000543898.5:c.1033-83A= ENSP00000444095.1:n.1033-83A=
ENST00000622132.4:c.1225-83A= ENSP00000478255.1:n.1225-83A=
NM_000927.4:c.1225-83A= NP_000918.2:n.1225-83A=
NM_001348944.1:c.1225-83A= NP_001335873.1:n.1225-83A=
NM_001348945.1:c.1435-83A= NP_001335874.1:n.1435-83A=
NM_001348946.1:c.1225-83A= NP_001335875.1:n.1225-83A=
NM_001348946.2:c.1225-83A= MANE Select NP_001335875.1:n.1225-83A=
NM_000927.5:c.1225-83A= NP_000918.2:n.1225-83A=
NM_001348944.2:c.1225-83A= NP_001335873.1:n.1225-83A=
NM_001348945.2:c.1435-83A= NP_001335874.1:n.1435-83A=