Canonical Allele Identifier: CA2617895576
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174746_21174747insACAG , CM000674.2:g.21174746_21174747insACAG GRCh38
NC_000012.11:g.21327680_21327681insACAG , CM000674.1:g.21327680_21327681insACAG GRCh37
NC_000012.10:g.21218947_21218948insACAG NCBI36
NG_011745.1:g.48553_48554insACAG , LRG_1022:g.48553_48554insACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+37_359+38insACAG MANE Select ENSP00000256958.2:n.359+37_359+38insACAG
ENST00000256958.2:c.359+37_359+38insACAG ENSP00000256958.2:n.359+37_359+38insACAG
ENST00000543498.5:c.426-2030_426-2029insACAG
NM_006446.4:c.359+37_359+38insACAG , LRG_1022t1:c.359+37_359+38insACAG NP_006437.3:n.359+37_359+38insACAG
NM_006446.5:c.359+37_359+38insACAG MANE Select NP_006437.3:n.359+37_359+38insACAG