Canonical Allele Identifier: CA162100586
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1002205

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87511858G>T , CM000669.2:g.87511858G>T GRCh38
NC_000007.13:g.87141174G>T , CM000669.1:g.87141174G>T GRCh37
NC_000007.12:g.86979110G>T NCBI36
NG_011513.1:g.206391C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.3283-2377C>A ENSP00000265724.3:p.=
ENST00000622132.5:c.3283-2377C>A MANE Select ENSP00000478255.1:p.=
ENST00000265724.7:c.3283-2377C>A ENSP00000265724.3:p.=
ENST00000475929.5:n.439-2377C>A
ENST00000488737.6:n.925-2377C>A
ENST00000543898.5:c.3091-2377C>A ENSP00000444095.1:p.=
ENST00000622132.4:c.3283-2377C>A ENSP00000478255.1:p.=
NM_000927.4:c.3283-2377C>A NP_000918.2:p.=
NM_001348944.1:c.3283-2377C>A NP_001335873.1:p.=
NM_001348945.1:c.3493-2377C>A NP_001335874.1:p.=
NM_001348946.1:c.3283-2377C>A NP_001335875.1:p.=
NM_001348946.2:c.3283-2377C>A MANE Select NP_001335875.1:p.=
NM_000927.5:c.3283-2377C>A NP_000918.2:p.=
NM_001348944.2:c.3283-2377C>A NP_001335873.1:p.=
NM_001348945.2:c.3493-2377C>A NP_001335874.1:p.=