Canonical Allele Identifier: CA2021009322
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215262_21215265delinsTAAG , CM000674.2:g.21215262_21215265delinsTAAG GRCh38
NC_000012.11:g.21368196_21368199delinsTAAG , CM000674.1:g.21368196_21368199delinsTAAG GRCh37
NC_000012.10:g.21259463_21259466delinsTAAG NCBI36
NG_011745.1:g.89069_89072delinsTAAG , LRG_1022:g.89069_89072delinsTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1857_1498-1854delinsTAAG MANE Select ENSP00000256958.2:n.1498-1857_1498-1854delinsTAAG
ENST00000256958.2:c.1498-1857_1498-1854delinsTAAG ENSP00000256958.2:n.1498-1857_1498-1854delinsTAAG
NM_006446.4:c.1498-1857_1498-1854delinsTAAG , LRG_1022t1:c.1498-1857_1498-1854delinsTAAG NP_006437.3:n.1498-1857_1498-1854delinsTAAG
NM_006446.5:c.1498-1857_1498-1854delinsTAAG MANE Select NP_006437.3:n.1498-1857_1498-1854delinsTAAG