Canonical Allele Identifier: CA2020990589
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176776T= , CM000674.2:g.21176776T= GRCh38
NC_000012.11:g.21329710T= , CM000674.1:g.21329710T= GRCh37
NC_000012.10:g.21220977T= NCBI36
NG_011745.1:g.50583T= , LRG_1022:g.50583T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.360T= MANE Select ENSP00000256958.2:p.Tyr120=
ENST00000256958.2:c.360T= ENSP00000256958.2:p.Tyr120=
ENST00000543498.5:c.426T=
NM_006446.4:c.360T= , LRG_1022t1:c.360T= NP_006437.3:p.Tyr120=
NM_006446.5:c.360T= MANE Select NP_006437.3:p.Tyr120=
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