Canonical Allele Identifier: CA2020990587
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176766G= , CM000674.2:g.21176766G= GRCh38
NC_000012.11:g.21329700G= , CM000674.1:g.21329700G= GRCh37
NC_000012.10:g.21220967G= NCBI36
NG_011745.1:g.50573G= , LRG_1022:g.50573G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.360-10G= MANE Select ENSP00000256958.2:n.360-10G=
ENST00000256958.2:c.360-10G= ENSP00000256958.2:n.360-10G=
ENST00000543498.5:c.426-10G=
NM_006446.4:c.360-10G= , LRG_1022t1:c.360-10G= NP_006437.3:n.360-10G=
NM_006446.5:c.360-10G= MANE Select NP_006437.3:n.360-10G=