Canonical Allele Identifier: CA233553701
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs55901008

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200595T>A , CM000674.2:g.21200595T>A GRCh38
NC_000012.11:g.21353529T>A , CM000674.1:g.21353529T>A GRCh37
NC_000012.10:g.21244796T>A NCBI36
NG_011745.1:g.74402T>A , LRG_1022:g.74402T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1058T>A MANE Select ENSP00000256958.2:p.Ile353Asn
ENST00000256958.2:c.1058T>A ENSP00000256958.2:p.Ile353Asn
NM_006446.4:c.1058T>A , LRG_1022t1:c.1058T>A NP_006437.3:p.Ile353Asn
NM_006446.5:c.1058T>A MANE Select NP_006437.3:p.Ile353Asn