Canonical Allele Identifier: CA2020990567
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940824933

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176684_21176689del , CM000674.2:g.21176684_21176689del GRCh38
NC_000012.11:g.21329618_21329623del , CM000674.1:g.21329618_21329623del GRCh37
NC_000012.10:g.21220885_21220890del NCBI36
NG_011745.1:g.50491_50496del , LRG_1022:g.50491_50496del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.360-92_360-87del MANE Select ENSP00000256958.2:n.360-92_360-87del
ENST00000256958.2:c.360-92_360-87del ENSP00000256958.2:n.360-92_360-87del
ENST00000543498.5:c.426-92_426-87del
NM_006446.4:c.360-92_360-87del , LRG_1022t1:c.360-92_360-87del NP_006437.3:n.360-92_360-87del
NM_006446.5:c.360-92_360-87del MANE Select NP_006437.3:n.360-92_360-87del