Canonical Allele Identifier: CA2020989814
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21175050_21175051delinsAG , CM000674.2:g.21175050_21175051delinsAG GRCh38
NC_000012.11:g.21327984_21327985delinsAG , CM000674.1:g.21327984_21327985delinsAG GRCh37
NC_000012.10:g.21219251_21219252delinsAG NCBI36
NG_011745.1:g.48857_48858delinsAG , LRG_1022:g.48857_48858delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+341_359+342delinsAG MANE Select ENSP00000256958.2:n.359+341_359+342delinsAG
ENST00000256958.2:c.359+341_359+342delinsAG ENSP00000256958.2:n.359+341_359+342delinsAG
ENST00000543498.5:c.426-1726_426-1725delinsAG
NM_006446.4:c.359+341_359+342delinsAG , LRG_1022t1:c.359+341_359+342delinsAG NP_006437.3:n.359+341_359+342delinsAG
NM_006446.5:c.359+341_359+342delinsAG MANE Select NP_006437.3:n.359+341_359+342delinsAG