Canonical Allele Identifier: CA2020989782
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174971_21174972delinsCG , CM000674.2:g.21174971_21174972delinsCG GRCh38
NC_000012.11:g.21327905_21327906delinsCG , CM000674.1:g.21327905_21327906delinsCG GRCh37
NC_000012.10:g.21219172_21219173delinsCG NCBI36
NG_011745.1:g.48778_48779delinsCG , LRG_1022:g.48778_48779delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+262_359+263delinsCG MANE Select ENSP00000256958.2:n.359+262_359+263delinsCG
ENST00000256958.2:c.359+262_359+263delinsCG ENSP00000256958.2:n.359+262_359+263delinsCG
ENST00000543498.5:c.426-1805_426-1804delinsCG
NM_006446.4:c.359+262_359+263delinsCG , LRG_1022t1:c.359+262_359+263delinsCG NP_006437.3:n.359+262_359+263delinsCG
NM_006446.5:c.359+262_359+263delinsCG MANE Select NP_006437.3:n.359+262_359+263delinsCG