Canonical Allele Identifier: CA2617895677
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174834_21174835insT , CM000674.2:g.21174834_21174835insT GRCh38
NC_000012.11:g.21327768_21327769insT , CM000674.1:g.21327768_21327769insT GRCh37
NC_000012.10:g.21219035_21219036insT NCBI36
NG_011745.1:g.48641_48642insT , LRG_1022:g.48641_48642insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+125_359+126insT MANE Select ENSP00000256958.2:n.359+125_359+126insT
ENST00000256958.2:c.359+125_359+126insT ENSP00000256958.2:n.359+125_359+126insT
ENST00000543498.5:c.426-1942_426-1941insT
NM_006446.4:c.359+125_359+126insT , LRG_1022t1:c.359+125_359+126insT NP_006437.3:n.359+125_359+126insT
NM_006446.5:c.359+125_359+126insT MANE Select NP_006437.3:n.359+125_359+126insT