Canonical Allele Identifier: CA2020989767
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174948_21174949delinsCT , CM000674.2:g.21174948_21174949delinsCT GRCh38
NC_000012.11:g.21327882_21327883delinsCT , CM000674.1:g.21327882_21327883delinsCT GRCh37
NC_000012.10:g.21219149_21219150delinsCT NCBI36
NG_011745.1:g.48755_48756delinsCT , LRG_1022:g.48755_48756delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+239_359+240delinsCT MANE Select ENSP00000256958.2:n.359+239_359+240delinsCT
ENST00000256958.2:c.359+239_359+240delinsCT ENSP00000256958.2:n.359+239_359+240delinsCT
ENST00000543498.5:c.426-1828_426-1827delinsCT
NM_006446.4:c.359+239_359+240delinsCT , LRG_1022t1:c.359+239_359+240delinsCT NP_006437.3:n.359+239_359+240delinsCT
NM_006446.5:c.359+239_359+240delinsCT MANE Select NP_006437.3:n.359+239_359+240delinsCT