Canonical Allele Identifier: CA2020975228
Gene: SLCO1B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21138592A= , CM000674.2:g.21138592A= GRCh38
NC_000012.11:g.21291526A= , CM000674.1:g.21291526A= GRCh37
NC_000012.10:g.21182793A= NCBI36
NG_011745.1:g.12399A= , LRG_1022:g.12399A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.-61-2922A= MANE Select ENSP00000256958.2:n.-61-2922A=
ENST00000256958.2:c.-61-2922A= ENSP00000256958.2:n.-61-2922A=
ENST00000543498.5:c.281-2922A=
ENST00000585342.5:c.485-2922A= ENSP00000467594.1:n.485-2922A=
ENST00000590779.5:c.491-2922A=
ENST00000592513.1:c.472-2922A=
NM_006446.4:c.-61-2922A= , LRG_1022t1:c.-61-2922A= NP_006437.3:n.-61-2922A=
NM_006446.5:c.-61-2922A= MANE Select NP_006437.3:n.-61-2922A=
Search 100 bp 5'
Search 100 bp 3'