Canonical Allele Identifier: CA2020991412
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178561_21178566delinsCTCTTA , CM000674.2:g.21178561_21178566delinsCTCTTA GRCh38
NC_000012.11:g.21331495_21331500delinsCTCTTA , CM000674.1:g.21331495_21331500delinsCTCTTA GRCh37
NC_000012.10:g.21222762_21222767delinsCTCTTA NCBI36
NG_011745.1:g.52368_52373delinsCTCTTA , LRG_1022:g.52368_52373delinsCTCTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.482-15_482-10delinsCTCTTA MANE Select ENSP00000256958.2:n.482-15_482-10delinsCTCTTA
ENST00000256958.2:c.482-15_482-10delinsCTCTTA ENSP00000256958.2:n.482-15_482-10delinsCTCTTA
NM_006446.4:c.482-15_482-10delinsCTCTTA , LRG_1022t1:c.482-15_482-10delinsCTCTTA NP_006437.3:n.482-15_482-10delinsCTCTTA
NM_006446.5:c.482-15_482-10delinsCTCTTA MANE Select NP_006437.3:n.482-15_482-10delinsCTCTTA