Canonical Allele Identifier: CA2020989622
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174624C= , CM000674.2:g.21174624C= GRCh38
NC_000012.11:g.21327558C= , CM000674.1:g.21327558C= GRCh37
NC_000012.10:g.21218825C= NCBI36
NG_011745.1:g.48431C= , LRG_1022:g.48431C=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.274C= MANE Select ENSP00000256958.2:p.His92=
ENST00000256958.2:c.274C= ENSP00000256958.2:p.His92=
ENST00000543498.5:c.426-2152C=
NM_006446.4:c.274C= , LRG_1022t1:c.274C= NP_006437.3:p.His92=
NM_006446.5:c.274C= MANE Select NP_006437.3:p.His92=