Canonical Allele Identifier: CA2020991402
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178544G= , CM000674.2:g.21178544G= GRCh38
NC_000012.11:g.21331478G= , CM000674.1:g.21331478G= GRCh37
NC_000012.10:g.21222745G= NCBI36
NG_011745.1:g.52351G= , LRG_1022:g.52351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.482-32G= MANE Select ENSP00000256958.2:n.482-32G=
ENST00000256958.2:c.482-32G= ENSP00000256958.2:n.482-32G=
NM_006446.4:c.482-32G= , LRG_1022t1:c.482-32G= NP_006437.3:n.482-32G=
NM_006446.5:c.482-32G= MANE Select NP_006437.3:n.482-32G=