Canonical Allele Identifier: CA384106486
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200511T>A , CM000674.2:g.21200511T>A GRCh38
NC_000012.11:g.21353445T>A , CM000674.1:g.21353445T>A GRCh37
NC_000012.10:g.21244712T>A NCBI36
NG_011745.1:g.74318T>A , LRG_1022:g.74318T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.974T>A MANE Select ENSP00000256958.2:p.Phe325Tyr
ENST00000256958.2:c.974T>A ENSP00000256958.2:p.Phe325Tyr
NM_006446.4:c.974T>A , LRG_1022t1:c.974T>A NP_006437.3:p.Phe325Tyr
NM_006446.5:c.974T>A MANE Select NP_006437.3:p.Phe325Tyr