Canonical Allele Identifier: CA2021009599
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215793_21215795delinsCTT , CM000674.2:g.21215793_21215795delinsCTT GRCh38
NC_000012.11:g.21368727_21368729delinsCTT , CM000674.1:g.21368727_21368729delinsCTT GRCh37
NC_000012.10:g.21259994_21259996delinsCTT NCBI36
NG_011745.1:g.89600_89602delinsCTT , LRG_1022:g.89600_89602delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1326_1498-1324delinsCTT MANE Select ENSP00000256958.2:n.1498-1326_1498-1324de...
ENST00000256958.2:c.1498-1326_1498-1324delinsCTT ENSP00000256958.2:n.1498-1326_1498-1324de...
NM_006446.4:c.1498-1326_1498-1324delinsCTT , LRG_1022t1:c.1498-1326_1498-1324delinsCTT NP_006437.3:n.1498-1326_1498-1324delinsCT...
NM_006446.5:c.1498-1326_1498-1324delinsCTT MANE Select NP_006437.3:n.1498-1326_1498-1324delinsCT...