Canonical Allele Identifier: CA2020991400
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178539T= , CM000674.2:g.21178539T= GRCh38
NC_000012.11:g.21331473T= , CM000674.1:g.21331473T= GRCh37
NC_000012.10:g.21222740T= NCBI36
NG_011745.1:g.52346T= , LRG_1022:g.52346T=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.482-37T= MANE Select ENSP00000256958.2:n.482-37T=
ENST00000256958.2:c.482-37T= ENSP00000256958.2:n.482-37T=
NM_006446.4:c.482-37T= , LRG_1022t1:c.482-37T= NP_006437.3:n.482-37T=
NM_006446.5:c.482-37T= MANE Select NP_006437.3:n.482-37T=