Canonical Allele Identifier: CA2021009761
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21216100_21216101delinsTG , CM000674.2:g.21216100_21216101delinsTG GRCh38
NC_000012.11:g.21369034_21369035delinsTG , CM000674.1:g.21369034_21369035delinsTG GRCh37
NC_000012.10:g.21260301_21260302delinsTG NCBI36
NG_011745.1:g.89907_89908delinsTG , LRG_1022:g.89907_89908delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1019_1498-1018delinsTG MANE Select ENSP00000256958.2:n.1498-1019_1498-1018delinsTG
ENST00000256958.2:c.1498-1019_1498-1018delinsTG ENSP00000256958.2:n.1498-1019_1498-1018delinsTG
NM_006446.4:c.1498-1019_1498-1018delinsTG , LRG_1022t1:c.1498-1019_1498-1018delinsTG NP_006437.3:n.1498-1019_1498-1018delinsTG
NM_006446.5:c.1498-1019_1498-1018delinsTG MANE Select NP_006437.3:n.1498-1019_1498-1018delinsTG