Canonical Allele Identifier: CA162111281
Gene: ABCB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11983225

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87532204T>C , CM000669.2:g.87532204T>C GRCh38
NC_000007.13:g.87161520T>C , CM000669.1:g.87161520T>C GRCh37
NC_000007.12:g.86999456T>C NCBI36
NG_011513.1:g.186045A>G

Transcript Alleles

HGVS Amino-acid change
NM_000927.4:c.2482-707A>G VV NP_000918.2:p.=
NM_001348944.1:c.2482-707A>G VV NP_001335873.1:p.=
NM_001348945.1:c.2692-707A>G VV NP_001335874.1:p.=
NM_001348946.1:c.2482-707A>G VV NP_001335875.1:p.=
ENST00000265724.7:c.2482-707A>G ENSP00000265724.3:p.=
ENST00000496821.5:n.110-707A>G
ENST00000543898.5:c.2290-707A>G ENSP00000444095.1:p.=
ENST00000622132.4:c.2482-707A>G ENSP00000478255.1:p.=