Canonical Allele Identifier: CA2020975241
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1231539679

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21138605G>A , CM000674.2:g.21138605G>A GRCh38
NC_000012.11:g.21291539G>A , CM000674.1:g.21291539G>A GRCh37
NC_000012.10:g.21182806G>A NCBI36
NG_011745.1:g.12412G>A , LRG_1022:g.12412G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.-61-2909G>A MANE Select ENSP00000256958.2:n.-61-2909G>A
ENST00000256958.2:c.-61-2909G>A ENSP00000256958.2:n.-61-2909G>A
ENST00000543498.5:c.281-2909G>A
ENST00000585342.5:c.485-2909G>A ENSP00000467594.1:n.485-2909G>A
ENST00000590779.5:c.491-2909G>A
ENST00000592513.1:c.472-2909G>A
NM_006446.4:c.-61-2909G>A , LRG_1022t1:c.-61-2909G>A NP_006437.3:n.-61-2909G>A
NM_006446.5:c.-61-2909G>A MANE Select NP_006437.3:n.-61-2909G>A