Canonical Allele Identifier: CA2020991413
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178561C= , CM000674.2:g.21178561C= GRCh38
NC_000012.11:g.21331495C= , CM000674.1:g.21331495C= GRCh37
NC_000012.10:g.21222762C= NCBI36
NG_011745.1:g.52368C= , LRG_1022:g.52368C=

Transcript Alleles

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