Canonical Allele Identifier: CA2020975199

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs1940261947

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21138579del , CM000674.2:g.21138579del	GRCh38
NC_000012.11:g.21291513del , CM000674.1:g.21291513del	GRCh37
NC_000012.10:g.21182780del	NCBI36
NG_011745.1:g.12386del , LRG_1022:g.12386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.-61-2935del MANE Select	ENSP00000256958.2:n.-61-2935del
ENST00000256958.2:c.-61-2935del	ENSP00000256958.2:n.-61-2935del
ENST00000543498.5:c.281-2935del
ENST00000585342.5:c.485-2935del	ENSP00000467594.1:n.485-2935del
ENST00000590779.5:c.491-2935del
ENST00000592513.1:c.472-2935del
NM_006446.4:c.-61-2935del , LRG_1022t1:c.-61-2935del	NP_006437.3:n.-61-2935del
NM_006446.5:c.-61-2935del MANE Select	NP_006437.3:n.-61-2935del