Canonical Allele Identifier: CA2020989639
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174653T= , CM000674.2:g.21174653T= GRCh38
NC_000012.11:g.21327587T= , CM000674.1:g.21327587T= GRCh37
NC_000012.10:g.21218854T= NCBI36
NG_011745.1:g.48460T= , LRG_1022:g.48460T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.303T= MANE Select ENSP00000256958.2:p.Cys101=
ENST00000256958.2:c.303T= ENSP00000256958.2:p.Cys101=
ENST00000543498.5:c.426-2123T=
NM_006446.4:c.303T= , LRG_1022t1:c.303T= NP_006437.3:p.Cys101=
NM_006446.5:c.303T= MANE Select NP_006437.3:p.Cys101=