Canonical Allele Identifier: CA2020989677
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174744C= , CM000674.2:g.21174744C= GRCh38
NC_000012.11:g.21327678C= , CM000674.1:g.21327678C= GRCh37
NC_000012.10:g.21218945C= NCBI36
NG_011745.1:g.48551C= , LRG_1022:g.48551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+35C= MANE Select ENSP00000256958.2:n.359+35C=
ENST00000256958.2:c.359+35C= ENSP00000256958.2:n.359+35C=
ENST00000543498.5:c.426-2032C=
NM_006446.4:c.359+35C= , LRG_1022t1:c.359+35C= NP_006437.3:n.359+35C=
NM_006446.5:c.359+35C= MANE Select NP_006437.3:n.359+35C=
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