Canonical Allele Identifier: CA2020991454
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178635C= , CM000674.2:g.21178635C= GRCh38
NC_000012.11:g.21331569C= , CM000674.1:g.21331569C= GRCh37
NC_000012.10:g.21222836C= NCBI36
NG_011745.1:g.52442C= , LRG_1022:g.52442C=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.541C= MANE Select ENSP00000256958.2:p.Arg181=
ENST00000256958.2:c.541C= ENSP00000256958.2:p.Arg181=
NM_006446.4:c.541C= , LRG_1022t1:c.541C= NP_006437.3:p.Arg181=
NM_006446.5:c.541C= MANE Select NP_006437.3:p.Arg181=