Canonical Allele Identifier: CA12663001
Gene: ABCB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4728702

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87551362A>T , CM000669.2:g.87551362A>T GRCh38
NC_000007.13:g.87180678A>T , CM000669.1:g.87180678A>T GRCh37
NC_000007.12:g.87018614A>T NCBI36
NG_011513.1:g.166887T>A

Transcript Alleles

HGVS Amino-acid change
NM_000927.4:c.1000-524T>A VV NP_000918.2:p.=
NM_001348944.1:c.1000-524T>A VV NP_001335873.1:p.=
NM_001348945.1:c.1210-524T>A VV NP_001335874.1:p.=
NM_001348946.1:c.1000-524T>A VV NP_001335875.1:p.=
ENST00000265724.7:c.1000-524T>A ENSP00000265724.3:p.=
ENST00000543898.5:c.808-524T>A ENSP00000444095.1:p.=
ENST00000622132.4:c.1000-524T>A ENSP00000478255.1:p.=