Canonical Allele Identifier: CA2020991407
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178552T= , CM000674.2:g.21178552T= GRCh38
NC_000012.11:g.21331486T= , CM000674.1:g.21331486T= GRCh37
NC_000012.10:g.21222753T= NCBI36
NG_011745.1:g.52359T= , LRG_1022:g.52359T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.482-24T= MANE Select ENSP00000256958.2:n.482-24T=
ENST00000256958.2:c.482-24T= ENSP00000256958.2:n.482-24T=
NM_006446.4:c.482-24T= , LRG_1022t1:c.482-24T= NP_006437.3:n.482-24T=
NM_006446.5:c.482-24T= MANE Select NP_006437.3:n.482-24T=
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