Canonical Allele Identifier: CA2021001553
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200851_21200852delinsCT , CM000674.2:g.21200851_21200852delinsCT GRCh38
NC_000012.11:g.21353785_21353786delinsCT , CM000674.1:g.21353785_21353786delinsCT GRCh37
NC_000012.10:g.21245052_21245053delinsCT NCBI36
NG_011745.1:g.74658_74659delinsCT , LRG_1022:g.74658_74659delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1135+179_1135+180delinsCT MANE Select ENSP00000256958.2:n.1135+179_1135+180delinsCT
ENST00000256958.2:c.1135+179_1135+180delinsCT ENSP00000256958.2:n.1135+179_1135+180delinsCT
NM_006446.4:c.1135+179_1135+180delinsCT , LRG_1022t1:c.1135+179_1135+180delinsCT NP_006437.3:n.1135+179_1135+180delinsCT
NM_006446.5:c.1135+179_1135+180delinsCT MANE Select NP_006437.3:n.1135+179_1135+180delinsCT