Canonical Allele Identifier: CA384104222
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21327588T>A (hg19) chr12:g.21174654T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174654T>A , CM000674.2:g.21174654T>A GRCh38
NC_000012.11:g.21327588T>A , CM000674.1:g.21327588T>A GRCh37
NC_000012.10:g.21218855T>A NCBI36
NG_011745.1:g.48461T>A , LRG_1022:g.48461T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.304T>A MANE Select ENSP00000256958.2:p.Phe102Ile
ENST00000256958.2:c.304T>A ENSP00000256958.2:p.Phe102Ile
ENST00000543498.5:c.426-2122T>A
NM_006446.4:c.304T>A , LRG_1022t1:c.304T>A NP_006437.3:p.Phe102Ile
NM_006446.5:c.304T>A MANE Select NP_006437.3:p.Phe102Ile
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