Canonical Allele Identifier: CA2020989747
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174904_21174907delinsTAAC , CM000674.2:g.21174904_21174907delinsTAAC GRCh38
NC_000012.11:g.21327838_21327841delinsTAAC , CM000674.1:g.21327838_21327841delinsTAAC GRCh37
NC_000012.10:g.21219105_21219108delinsTAAC NCBI36
NG_011745.1:g.48711_48714delinsTAAC , LRG_1022:g.48711_48714delinsTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+195_359+198delinsTAAC MANE Select ENSP00000256958.2:n.359+195_359+198delinsTAAC
ENST00000256958.2:c.359+195_359+198delinsTAAC ENSP00000256958.2:n.359+195_359+198delinsTAAC
ENST00000543498.5:c.426-1872_426-1869delinsTAAC
NM_006446.4:c.359+195_359+198delinsTAAC , LRG_1022t1:c.359+195_359+198delinsTAAC NP_006437.3:n.359+195_359+198delinsTAAC
NM_006446.5:c.359+195_359+198delinsTAAC MANE Select NP_006437.3:n.359+195_359+198delinsTAAC